Exact Mass: 185.9987

Exact Mass Matches: 185.9987

Found 127 metabolites which its exact mass value is equals to given mass value 185.9987, within given mass tolerance error 0.01 dalton. Try search metabolite list with more accurate mass tolerance error 0.001 dalton.

D-Glycerate 3-phosphate

(2R)-2-Hydroxy-3-(phosphonatooxy)propanoic acid

C3H7O7P (185.9929)


3-phospho-d-glyceric acid, also known as 3-phosphoglycerate or D-glycerate 3-phosphate, belongs to sugar acids and derivatives class of compounds. Those are compounds containing a saccharide unit which bears a carboxylic acid group. 3-phospho-d-glyceric acid is soluble (in water) and a moderately acidic compound (based on its pKa). 3-phospho-d-glyceric acid can be found in a number of food items such as towel gourd, orange mint, guava, and mulberry, which makes 3-phospho-d-glyceric acid a potential biomarker for the consumption of these food products. 3-phospho-d-glyceric acid can be found primarily in saliva. 3-phospho-d-glyceric acid exists in all living species, ranging from bacteria to humans. (2R)-2-Hydroxy-3-(phosphonatooxy)propanoate, also known as 3-phospho-(R)-glycerate or D-glycerate 3-phosphate, belongs to the class of organic compounds known as sugar acids and derivatives. Sugar acids and derivatives are compounds containing a saccharide unit which bears a carboxylic acid group (2R)-2-Hydroxy-3-(phosphonatooxy)propanoate is a drug (2R)-2-hydroxy-3-(phosphonatooxy)propanoate has been detected, but not quantified, in several different foods, such as poppies, small-leaf lindens, lupines, pomegranates, and kombus. These are compounds containing a saccharide unit which bears a carboxylic acid group.

   

4-Chlorophenoxyacetic acid

4-Chlorophenoxyacetic acid, potassium salt

C8H7ClO3 (186.0084)


CONFIDENCE standard compound; INTERNAL_ID 1191; DATASET 20200303_ENTACT_RP_MIX499; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3757; ORIGINAL_PRECURSOR_SCAN_NO 3752 CONFIDENCE standard compound; INTERNAL_ID 1191; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3829; ORIGINAL_PRECURSOR_SCAN_NO 3825 CONFIDENCE standard compound; INTERNAL_ID 1191; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4159; ORIGINAL_PRECURSOR_SCAN_NO 4154 CONFIDENCE standard compound; INTERNAL_ID 1191; DATASET 20200303_ENTACT_RP_MIX499; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 3737; ORIGINAL_PRECURSOR_SCAN_NO 3736 CONFIDENCE standard compound; INTERNAL_ID 1191; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4074; ORIGINAL_PRECURSOR_SCAN_NO 4072 CONFIDENCE standard compound; INTERNAL_ID 1191; DATASET 20200303_ENTACT_RP_MIX505; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 4080; ORIGINAL_PRECURSOR_SCAN_NO 4076 KEIO_ID C151

   

2-Phospho-D-glyceric acid

(2R)-3-Hydroxy-2-(phosphonooxy)propanoic acid

C3H7O7P (185.9929)


2-Phosphoglyceric acid (2PG), or 2-phosphoglycerate, is a glyceric acid which serves as the substrate in the ninth step of glycolysis. It is catalyzed by enolase into phosphoenolpyruvate (PEP), the penultimate step in the conversion of glucose to pyruvate.; 2-Phosphoglyceric acid (2PGA) is a glyceric acid which serves as the substrate in the ninth step of glycolysis. It is catalyzed by enolase into phosphoenolpyruvate (PEP), the penultimate step in the conversion of glucose to pyruvate. Enolase catalyzes the beta-elimination reaction in a stepwise manner wherein OH- is eliminated from C3 of a discrete carbanion (enolate) intermediate. This intermediate is created by removal of the proton from C2 of 2PGA by a base in the active site. (PMID: 8994873, Wikipedia). 2-Phosphoglycerate is found in rice. 2-Phospho-D-glycerate or 2PG is an intermediate in gluconeogenesis. It is a glyceric acid which serves as the substrate in the ninth step of glycolysis. 2PG is converted by enolase into phosphoenolpyruvate (PEP), the penultimate step in the conversion of glucose to pyruvate. More specifically, 2PG can be generated from Glycerate-3-phosphate via phosphoglycerate mutase or from phosphoenolpyrvate via alpha enolase. KEIO_ID P029

   

4-Sulfobenzaldehyde

4-formylbenzenesulfonic acid

C7H6O4S (185.9987)


   

2-hydroxyethyl-CoM

2-(2-Hydroxyethylsulfanyl)ethanesulfonic acid

C4H10O4S2 (186.002)


   

3-phosphoglycerate

3-(Dihydrogen phosphoric acid)glyceric acid

C3H7O7P (185.9929)


3-Phosphoglyceric acid, also known as 3PG, belongs to the class of organic compounds known as sugar acids and derivatives. Sugar acids and derivatives are compounds containing a saccharide unit which bears a carboxylic acid group. 3PG is the conjugate acid of glycerate 3-phosphate (GP or G3P). It is a solid that is soluble in water. 3-Phosphoglyceric acid exists in all living species, ranging from bacteria to humans. The glycerate is a biochemically significant metabolic intermediate in both glycolysis and the Calvin cycle. This is the first compound formed during the C3 or Calvin cycle. Glycerate 3-phosphate is also a precursor for serine, which, in turn, can create cysteine and glycine through the homocysteine cycle. Within humans, 3-phosphoglyceric acid participates in a number of enzymatic reactions. In particular, 3-phosphoglyceric acid can be biosynthesized from glyceric acid 1,3-biphosphate, which is mediated by the enzyme phosphoglycerate kinase 1. In addition, 3PG can be converted into 2-phospho-D-glyceric acid, which is catalyzed by the enzyme phosphoglycerate mutase 2. 3-phosphoglyceric acid is involved in the Warburg effect (aerobic glycolysis), a metabolic shift that is a hallmark of cancer (PMID: 29362480). 3-phosphoglyceric acid (3PG) is a 3-carbon molecule that is a metabolic intermediate in both glycolysis and the Calvin cycle. This chemical is often termed PGA when referring to the Calvin cycle. In the Calvin cycle, two glycerate 3-phosphate molecules are reduced to form two molecules of glyceraldehyde 3-phosphate (GALP). (wikipedia) [HMDB] KEIO_ID P028

   

2-Phosphoglyceric acid

3-Hydroxy-2-(phosphonooxy)propanoic acid

C3H7O7P (185.9929)


2-Phosphoglyceric acid (2PGA) is a glyceric acid which serves as the substrate in the ninth step of glycolysis. It is catalyzed by enolase into phosphoenolpyruvate (PEP), the penultimate step in the conversion of glucose to pyruvate. Enolase catalyzes the beta-elimination reaction in a stepwise manner wherein OH- is eliminated from C3 of a discrete carbanion (enolate) intermediate. This intermediate is created by removal of the proton from C2 of 2PGA by a base in the active site. (PMID: 8994873, Wikipedia) [HMDB] 2-Phosphoglyceric acid (2PGA) is a glyceric acid which serves as the substrate in the ninth step of glycolysis. It is catalyzed by enolase into phosphoenolpyruvate (PEP), the penultimate step in the conversion of glucose to pyruvate. Enolase catalyzes the beta-elimination reaction in a stepwise manner wherein OH- is eliminated from C3 of a discrete carbanion (enolate) intermediate. This intermediate is created by removal of the proton from C2 of 2PGA by a base in the active site (PMID: 8994873, Wikipedia). 2-Phosphoglyceric acid. CAS Common Chemistry. CAS, a division of the American Chemical Society, n.d. https://commonchemistry.cas.org/detail?cas_rn=2553-59-5 (retrieved 2024-11-04) (CAS RN: 2553-59-5). Licensed under the Attribution-Noncommercial 4.0 International License (CC BY-NC 4.0).

   

8-Chloroxanthine

1H-Purine-2,6-dione, 8-chloro-3,7-dihydro- (9CI)

C5H3ClN4O2 (185.9945)


8-Chloroxanthine is a derivative of xanthine, found occasionally in human urine. 8-Chloroxanthine originates from the metabolism of methylxanthines (caffeine, theophylline and theobromine. Purine derivatives in urinary calculi could be considered markers of abnormal purine metabolism. The content of a purine derivative in stone depends on its average urinary excretion in the general population, similarity to the chemical structure of uric acid, and content of the latter in stone. This suggests that purines in stones represent a solid solution with uric acid as solvent. It is also plausible that methylxanthines, ubiquitous components of the diet and drugs, are involved in the pathogenesis of urolithiasis. Caffeine is metabolized via successive pathways mainly catalyzed by CYP1A2, xanthine oxidase or N-acetyltransferase-2 to give 14 different metabolites. CYP1A2 activity shows an inter-individual variability among the population. CYP1A2, an isoform of the CYP1A cytochrome P450 super-family, is involved in the metabolism of many drugs and plays a potentially important role in the induction of chemical carcinogenesis. (PMID: 11712316, 15833286, 3506820, 15013152) [HMDB] 8-Chloroxanthine is a derivative of xanthine, found occasionally in human urine. 8-Chloroxanthine originates from the metabolism of methylxanthines (caffeine, theophylline and theobromine. Purine derivatives in urinary calculi could be considered markers of abnormal purine metabolism. The content of a purine derivative in stone depends on its average urinary excretion in the general population, similarity to the chemical structure of uric acid, and content of the latter in stone. This suggests that purines in stones represent a solid solution with uric acid as solvent. It is also plausible that methylxanthines, ubiquitous components of the diet and drugs, are involved in the pathogenesis of urolithiasis. Caffeine is metabolized via successive pathways mainly catalyzed by CYP1A2, xanthine oxidase or N-acetyltransferase-2 to give 14 different metabolites. CYP1A2 activity shows an inter-individual variability among the population. CYP1A2, an isoform of the CYP1A cytochrome P450 super-family, is involved in the metabolism of many drugs and plays a potentially important role in the induction of chemical carcinogenesis. (PMID: 11712316, 15833286, 3506820, 15013152).

   

Diethyldithiophosphate

O,O-Diethyl dithiophosphate, potassium salt

C4H11O2PS2 (185.9938)


Diethyldithiophosphate, also known as O,O-diethyl dithiophosphate, potassium salt, is classified as a member of the phosphorodithioic acid O,O-diesters. Phosphorodithioic acid O,O-diesters are organooxygen compounds that contain a phosphorodithioic acid, which is O,O-disubstituted by an organyl group. Diethyl dithiophosphate is considered to be practically insoluble (in water) and acidic. Diethyldithiophosphate is the processor for production of the organophosphate insecticide Terbufos. (ChemoSummarizer)

   

1-Fluoro-2,4-dinitrobenzene

2,4-Dinitrobenzene fluoride

C6H3FN2O4 (186.0077)


   

1-Fluoro-2,3-dinitrobenzene

1-Fluoro-2,3-dinitrobenzene

C6H3FN2O4 (186.0077)


   

3-Chloro-4-hydroxy-5-methoxybenzaldehyde

3-Chloro-4-hydroxy-5-methoxybenzaldehyde

C8H7ClO3 (186.0084)


D002491 - Central Nervous System Agents > D000927 - Anticonvulsants D020011 - Protective Agents > D016587 - Antimutagenic Agents D020011 - Protective Agents > D000975 - Antioxidants

   

5-(Methoxycarbonyl)thiophene-2-carboxylic acid

5-(METHOXYCARBONYL)THIOPHENE-2-CARBOXYLIC ACID

C7H6O4S (185.9987)


   

Hexafluorobenzene

1,2,3,4,5,6-Hexafluorobenzene

C6F6 (185.9904)


   

3-phosphoglycerate

3-Phosphoglyceric acid

C3H7O7P (185.9929)


A monophosphoglyceric acid having the phospho group at the 3-position. It is an intermediate in metabolic pathways like glycolysis and calvin cycle.

   
   

3-chloro-2,6-dihydroxy-4-methylbenzaldehyde

3-chloro-2,6-dihydroxy-4-methylbenzaldehyde

C8H7ClO3 (186.0084)


   

2-CHLORO-4-HYDROXY-5-METHOXYBENZALDEHYDE

2-CHLORO-4-HYDROXY-5-METHOXYBENZALDEHYDE

C8H7ClO3 (186.0084)


   

3-Chloro-4-methoxybenzoic acid

3-Chloro-4-methoxybenzoic acid

C8H7ClO3 (186.0084)


   

2-chloro-5-methoxy-3-methylcyclohexa-2,5-diene-1,4-dione

2-chloro-5-methoxy-3-methylcyclohexa-2,5-diene-1,4-dione

C8H7ClO3 (186.0084)


   

3-Chloro-4-hydroxyphenylacetic acid

3-Chloro-4-hydroxyphenylacetic acid

C8H7ClO3 (186.0084)


   

D-(-)-3-Phosphoglyceric acid

D-(-)-3-Phosphoglyceric acid

C3H7O7P (185.9929)


   

3-Phosphoglyceric acid

3-Phospho-D-glyceric acid

C3H7O7P (185.9929)


The D-enantiomer of 3-phosphoglyceric acid

   

4-CPA

4-CHLOROPHENOXYACETIC ACID

C8H7ClO3 (186.0084)


   

Chloratranol

Chloratranol

C8H7ClO3 (186.0084)


   

2-formylbenzenesulfonate

2-Formylbenzenesulfonic acid

C7H6O4S (185.9987)


CONFIDENCE standard compound; INTERNAL_ID 766; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2226; ORIGINAL_PRECURSOR_SCAN_NO 2225 CONFIDENCE standard compound; INTERNAL_ID 766; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2215; ORIGINAL_PRECURSOR_SCAN_NO 2214 CONFIDENCE standard compound; INTERNAL_ID 766; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2174; ORIGINAL_PRECURSOR_SCAN_NO 2173 CONFIDENCE standard compound; INTERNAL_ID 766; DATASET 20200303_ENTACT_RP_MIX506; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2219; ORIGINAL_PRECURSOR_SCAN_NO 2218 CONFIDENCE standard compound; INTERNAL_ID 766; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2175; ORIGINAL_PRECURSOR_SCAN_NO 2174 CONFIDENCE standard compound; INTERNAL_ID 766; DATASET 20200303_ENTACT_RP_MIX507; DATA_PROCESSING MERGING RMBmix ver. 0.2.7; DATA_PROCESSING PRESCREENING Shinyscreen ver. 0.8.0; ORIGINAL_ACQUISITION_NO 2187; ORIGINAL_PRECURSOR_SCAN_NO 2186

   

2-phosphoglycerate

2-phosphoglycerate

C3H7O7P (185.9929)


   

2-phosphoglyceric acid

2-phosphoglyceric acid

C3H7O7P (185.9929)


A monophosphoglyceric acid having the phospho group at the 2-position.

   

8-Chloroxanthine

1H-Purine-2,6-dione, 8-chloro-3,7-dihydro- (9CI)

C5H3ClN4O2 (185.9945)


   

2H-Benzimidazole-2-thione,5,6-difluoro-1,3-dihydro-(9CI)

2H-Benzimidazole-2-thione,5,6-difluoro-1,3-dihydro-(9CI)

C7H4F2N2S (186.0063)


   

Benzoyl chloride, 3-hydroxy-4-methoxy- (9CI)

Benzoyl chloride, 3-hydroxy-4-methoxy- (9CI)

C8H7ClO3 (186.0084)


   

3-chlorophenylthiourea

3-chlorophenylthiourea

C7H7ClN2S (186.0018)


   

4-Chlorophenylglyoxal hydrate

4-Chlorophenylglyoxal hydrate

C8H7ClO3 (186.0084)


   

P-chloro mandelic acid

P-chloro mandelic acid

C8H7ClO3 (186.0084)


   

Methyl 2-chloro-3-hydroxybenzoate

Methyl 2-chloro-3-hydroxybenzoate

C8H7ClO3 (186.0084)


   

Methyl 2-chloro-4-hydroxybenzoate

Methyl 2-chloro-4-hydroxybenzoate

C8H7ClO3 (186.0084)


   

Benzoic acid, 3-sulfino-

Benzoic acid, 3-sulfino-

C7H6O4S (185.9987)


   

4-methoxyphenyl chloroformate

4-methoxyphenyl chloroformate

C8H7ClO3 (186.0084)


   

Methyl 3-chloro-4-hydroxybenzoate

Methyl 3-chloro-4-hydroxybenzoate

C8H7ClO3 (186.0084)


   

Benzaldehyde,2-chloro-4-hydroxy-3-methoxy-

Benzaldehyde,2-chloro-4-hydroxy-3-methoxy-

C8H7ClO3 (186.0084)


   

Methyl 2-chloro-5-hydroxybenzoate

Methyl 2-chloro-5-hydroxybenzoate

C8H7ClO3 (186.0084)


   

2-(5-chloro-2-hydroxyphenyl)acetic acid

2-(5-chloro-2-hydroxyphenyl)acetic acid

C8H7ClO3 (186.0084)


   

(2R)-(4-Chlorophenyl)(hydroxy)acetic acid

(2R)-(4-Chlorophenyl)(hydroxy)acetic acid

C8H7ClO3 (186.0084)


   

(S)-2-(3-CHLOROPHENYL)-2-HYDROXYACETIC ACID

(S)-2-(3-CHLOROPHENYL)-2-HYDROXYACETIC ACID

C8H7ClO3 (186.0084)


   

3-(3,4-DICHLOROPHENYL)-1-PROPENE

3-(3,4-DICHLOROPHENYL)-1-PROPENE

C9H8Cl2 (186.0003)


   

1-(5-Chloro-2,4-dihydroxyphenyl)ethanone

1-(5-Chloro-2,4-dihydroxyphenyl)ethanone

C8H7ClO3 (186.0084)


   

2-Chloromandelic acid

2-Chloromandelic acid

C8H7ClO3 (186.0084)


   

4-Chloro-2-methoxybenzoic acid

4-Chloro-2-methoxybenzoic acid

C8H7ClO3 (186.0084)


   

2-amino-4,6-difluorobenzothiazole

2-amino-4,6-difluorobenzothiazole

C7H4F2N2S (186.0063)


   

Methyl 5-chlorosalicylate

Methyl 5-chloro-2-hydroxybenzoate

C8H7ClO3 (186.0084)


   

3-chlorophenoxyacetic acid

3-chlorophenoxyacetic acid

C8H7ClO3 (186.0084)


   

3,4-dihydroxyphenacyl chloride

2-Chloro-3,4-dihydroxyacetophenone

C8H7ClO3 (186.0084)


   

2-Aminobenzothiazole Hydrochloride

2-Aminobenzothiazole Hydrochloride

C7H7ClN2S (186.0018)


   

(2,2-dichlorocyclopropyl)benzene

(2,2-dichlorocyclopropyl)benzene

C9H8Cl2 (186.0003)


   
   

(2-methoxyphenyl) carbonochloridate

(2-methoxyphenyl) carbonochloridate

C8H7ClO3 (186.0084)


   

4-(2-ETHOXYETHOXY)ANILINE

4-(2-ETHOXYETHOXY)ANILINE

C9H8Cl2 (186.0003)


   

(S)-2-Chloromandelic acid

(S)-2-Chloromandelic acid

C8H7ClO3 (186.0084)


   

(7-Chloro-1,3-benzodioxol-5-yl)methanol

(7-Chloro-1,3-benzodioxol-5-yl)methanol

C8H7ClO3 (186.0084)


   

5-methylthiophene-2,3-dicarboxylic acid

5-methylthiophene-2,3-dicarboxylic acid

C7H6O4S (185.9987)


   

2-Chloro-5-methoxybenzoic acid

2-Chloro-5-methoxybenzoic acid

C8H7ClO3 (186.0084)


   

2-chlorophenoxyacetic acid

2-chlorophenoxyacetic acid

C8H7ClO3 (186.0084)


   

4-chloro-5,7-dihydro-2-methylthieno[3,4-d]pyrimidine

4-chloro-5,7-dihydro-2-methylthieno[3,4-d]pyrimidine

C7H7ClN2S (186.0018)


   

4-chloro-3-hydroxyphenylacetic acid

4-chloro-3-hydroxyphenylacetic acid

C8H7ClO3 (186.0084)


   

2,3-dihydrothieno[3,4-b][1,4]dioxine-5-carboxylic acid

2,3-dihydrothieno[3,4-b][1,4]dioxine-5-carboxylic acid

C7H6O4S (185.9987)


   

Methyl 3-chloro-2-hydroxybenzoate

Methyl 3-chloro-2-hydroxybenzoate

C8H7ClO3 (186.0084)


   

(R)-(-)-2-METHYL-2,4-PENTANEDIOL

(R)-(-)-2-METHYL-2,4-PENTANEDIOL

C8H7ClO3 (186.0084)


   

1-Chloro-6,7-dihydrobenzo[c]thiophen-4(5H)-one

1-Chloro-6,7-dihydrobenzo[c]thiophen-4(5H)-one

C8H7ClOS (185.9906)


   

3-Thienylmalonic acid

3-Thienylmalonic acid

C7H6O4S (185.9987)


   

6-chloropiperonyl alcohol

6-chloropiperonyl alcohol

C8H7ClO3 (186.0084)


   

2-Chloro-6-methoxybenzoic acid

2-Chloro-6-methoxybenzoic acid

C8H7ClO3 (186.0084)


   

2-AMino-4,7-difluorobenzothiazole

2-AMino-4,7-difluorobenzothiazole

C7H4F2N2S (186.0063)


   

2-Chloro-3-hydroxy-4-methoxybenzaldehyde

2-Chloro-3-hydroxy-4-methoxybenzaldehyde

C8H7ClO3 (186.0084)


   

4-Chloromandelic acid

4-Chloromandelic acid

C8H7ClO3 (186.0084)


   

3-CHLOROPHENYLGLYOXAL HYDRATE

3-CHLOROPHENYLGLYOXAL HYDRATE

C8H7ClO3 (186.0084)


   

1,2,2,2-TETRAFLUOROETHYL TRIFLUOROMETHYL ETHER

1,2,2,2-TETRAFLUOROETHYL TRIFLUOROMETHYL ETHER

C3HF7O (185.9916)


   

Cyclohexylmagnesium Bromide

Cyclohexylmagnesium Bromide

C6H11BrMg (185.9895)


   

Potassium cinnamate

Potassium cinnamate

C9H7KO2 (186.0083)


   

Perfluorobenzene

Hexafluorobenzene

C6F6 (185.9904)


   

S-METHYL 4,4,4-TRIFLUORO-3-OXOTHIO-BUTYR ATE,

S-METHYL 4,4,4-TRIFLUORO-3-OXOTHIO-BUTYR ATE,

C5H5F3O2S (185.9962)


   

3,4-Dinitrofluorobenzene

3,4-Dinitrofluorobenzene

C6H3FN2O4 (186.0077)


   

2-Chloro-5-hydroxy-4-methylbenzoic acid

2-Chloro-5-hydroxy-4-methylbenzoic acid

C8H7ClO3 (186.0084)


   

p-Hydroxyphenyl chloroacetate

p-Hydroxyphenyl chloroacetate

C8H7ClO3 (186.0084)


   

1-(2-Chlorophenyl)-2-thiourea

1-(2-Chlorophenyl)-2-thiourea

C7H7ClN2S (186.0018)


   

ETHANONE, 2-CHLORO-1-(2,4-DIHYDROXYPHENYL)-

ETHANONE, 2-CHLORO-1-(2,4-DIHYDROXYPHENYL)-

C8H7ClO3 (186.0084)


   

2-chloro-2-5-dihydroxyacetophenone

2-chloro-2-5-dihydroxyacetophenone

C8H7ClO3 (186.0084)


   

6-Chlorovanillin

6-Chlorovanillin

C8H7ClO3 (186.0084)


   

3-Chloro-2-methoxybenzoicacid

3-Chloro-2-methoxybenzoicacid

C8H7ClO3 (186.0084)


   

4-methylsulfanylbenzoyl chloride

4-methylsulfanylbenzoyl chloride

C8H7ClOS (185.9906)


   

(S)-2-(4-Chlorophenyl)-2-hydroxyacetic acid

(S)-2-(4-Chlorophenyl)-2-hydroxyacetic acid

C8H7ClO3 (186.0084)


   

5-Chloro-2-hydroxy-3-methoxybenzaldehyde

5-Chloro-2-hydroxy-3-methoxybenzaldehyde

C8H7ClO3 (186.0084)


   

3-Chloro-4-Methoxysalicylaldehyde

3-Chloro-4-Methoxysalicylaldehyde

C8H7ClO3 (186.0084)


   

(R)-2-(2-Chlorophenyl)-2-hydroxyacetic acid

(R)-2-(2-Chlorophenyl)-2-hydroxyacetic acid

C8H7ClO3 (186.0084)


   

5-AMINO-1,3-BENZOTHIAZOLE HCL

5-AMINO-1,3-BENZOTHIAZOLE HCL

C7H7ClN2S (186.0018)


   

4-CHLOROPHENYLTHIOUREA

4-CHLOROPHENYLTHIOUREA

C7H7ClN2S (186.0018)


   

5-Chloro-2-methoxybenzoic acid

5-Chloro-2-methoxybenzoic acid

C8H7ClO3 (186.0084)


   

1-(4-CHLOROPHENYL)-2-MERCAPTOETHANONE

1-(4-CHLOROPHENYL)-2-MERCAPTOETHANONE

C8H7ClOS (185.9906)


   

2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE-2-CARBOXYLIC ACID

2,3-DIHYDROTHIENO[3,4-B][1,4]DIOXINE-2-CARBOXYLIC ACID

C7H6O4S (185.9987)


   

METHYL 4-CHLORO-4,4-DIFLUOROACETOACETATE

METHYL 4-CHLORO-4,4-DIFLUOROACETOACETATE

C5H5ClF2O3 (185.9895)


   

(phenylthio)acetyl chloride

(phenylthio)acetyl chloride

C8H7ClOS (185.9906)


   

3-(3,5-DICHLOROPHENYL)-1-PROPENE

3-(3,5-DICHLOROPHENYL)-1-PROPENE

C9H8Cl2 (186.0003)


   

3-Chloro-5-methoxybenzoic acid

3-Chloro-5-methoxybenzoic acid

C8H7ClO3 (186.0084)


   

4-Chloro-3-methoxybenzoic acid

4-Chloro-3-methoxybenzoic acid

C8H7ClO3 (186.0084)


   

2,5-Difluoro-4-thiocyanatoaniline

2,5-Difluoro-4-thiocyanatoaniline

C7H4F2N2S (186.0063)


   

5,7-DIFLUOROBENZO[D]THIAZOL-2-AMINE

5,7-DIFLUOROBENZO[D]THIAZOL-2-AMINE

C7H4F2N2S (186.0063)


   

N,N-(1,4-PHENYLENE)BIS(ACETOACETAMIDE)

N,N-(1,4-PHENYLENE)BIS(ACETOACETAMIDE)

C8H7ClOS (185.9906)


   

2-Chloro-3-methoxybenzoic acid

2-Chloro-3-methoxybenzoic acid

C8H7ClO3 (186.0084)


   

Methyl 3-chloro-5-hydroxybenzoate

Methyl 3-chloro-5-hydroxybenzoate

C8H7ClO3 (186.0084)


   

2-amino-5,6-difluorobenzothiazole

2-amino-5,6-difluorobenzothiazole

C7H4F2N2S (186.0063)


   

p-tolyl chlorothionoformate

p-tolyl chlorothionoformate

C8H7ClOS (185.9906)


   

3-Chlorophenylglycolic Acid

3-Chlorophenylglycolic Acid

C8H7ClO3 (186.0084)


   

Propane,1,1-thiobis[3-chloro- (9CI)

Propane,1,1-thiobis[3-chloro- (9CI)

C6H12Cl2S (186.0037)


   

2-Chloro-4-methoxybenzoic acid

2-Chloro-4-methoxybenzoic acid

C8H7ClO3 (186.0084)


   

Benzoic acid,4-chloro-2-hydroxy-, methyl ester

Benzoic acid,4-chloro-2-hydroxy-, methyl ester

C8H7ClO3 (186.0084)


   

Methyl 4-chloro-3-hydroxybenzoate

Methyl 4-chloro-3-hydroxybenzoate

C8H7ClO3 (186.0084)


   

POTASSIUM TRIFLUORO(PYRIMIDIN-2-YL)BORATE

POTASSIUM TRIFLUORO(PYRIMIDIN-2-YL)BORATE

C4H3BF3KN2 (185.9978)


   

2-Bromo-1-ethylpyridin-1-ium

2-Bromo-1-ethylpyridin-1-ium

C7H9BrN+ (185.9918)


   

1-Propanol, 1,1,2,2,3,3,3-heptafluoro-

1-Propanol, 1,1,2,2,3,3,3-heptafluoro-

C3HF7O (185.9916)


   

2-Amino-5-chlorophenyl carbonate

2-Amino-5-chlorophenyl carbonate

C7H5ClNO3- (185.9958)


   

Alloxanoic acid

Alloxanoic acid

C5H2N2O6 (185.9913)


   

Dithiophosphoric acid diethyl ester

Dithiophosphoric acid diethyl ester

C4H11O2PS2 (185.9938)


   

2-Phospho-D-glyceric acid

2-Phospho-D-glyceric acid

C3H7O7P (185.9929)


A 2-phosphoglyceric acid in which the glyceric acid moiety has D (R) configuration.

   

4-formylbenzenesulfonic acid

4-formylbenzenesulfonic acid

C7H6O4S (185.9987)


   

1-Fluoro-2,4-dinitrobenzene

1-Fluoro-2,4-dinitrobenzene

C6H3FN2O4 (186.0077)


   

Diethyl dithiophosphoric acid

Diethyl dithiophosphoric acid

C4H11O2PS2 (185.9938)


   

(3-chloro-4-hydroxyphenyl)acetic acid

(3-chloro-4-hydroxyphenyl)acetic acid

C8H7ClO3 (186.0084)


A hydroxy monocarboxylic acid that is acetic acid in which one of the methyl hydrogens is replaced by a 3-chloro-4-hydroxyphenyl group. It is a major chlorinated metabolite of chlorotyrosine.

   

Phosphoglyceric acid

Phosphoglyceric acid

C3H7O7P (185.9929)