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Merck

T33006

Sigma-Aldrich

(Phenylthio)acetic acid

96%

Sinónimos:

(Phenylmercapto)acetic acid, S-Phenylthioglycolic acid, Thiophenoxyacetic acid

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About This Item

Fórmula lineal:
C6H5SCH2COOH
Número de CAS:
Peso molecular:
168.21
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

assay

96%

mp

60-63 °C (lit.)

SMILES string

OC(=O)CSc1ccccc1

InChI

1S/C8H8O2S/c9-8(10)6-11-7-4-2-1-3-5-7/h1-5H,6H2,(H,9,10)

InChI key

MOTOSAGBNXXRRE-UHFFFAOYSA-N

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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


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John F Bower et al.
Organic & biomolecular chemistry, 4(10), 1868-1877 (2006-05-12)
A structurally representative series of 1,2- and 1,3-cyclic sulfamidates react with enolates derived from methyl alpha-phenylthioacetate 9b to give 5- and 6-substituted alpha-phenylthio lactams 20-24. These products provide, via the corresponding sulfoxides, an entry to alpha,beta-unsaturated lactams e.g. 12, 27
Sub-banding and fine structure of serum lactate dehydrogenase isoenzymes induced by sulfur compounds.
L L Gershbein
Biochemical and biophysical research communications, 101(4), 1116-1122 (1981-08-31)
Rui Zhang et al.
Bioorganic & medicinal chemistry letters, 19(4), 1101-1104 (2009-01-27)
Synthesis and SAR of para-alkylthiophenoxyacetic acids is described. Achiral compounds 30, 31 and 32 were identified as potent and selective PPARdelta agonists.
L Rodrigo et al.
Chemico-biological interactions, 119-120, 263-275 (1999-07-27)
The existence of two or more enzyme forms with paraoxonase activity has been reported in sheep, rabbit, human and rat serum and recently in mouse and rat liver. In this study we describe the presence of two peaks with paraoxonase
A Q Zhang et al.
Chemosphere, 36(15), 3033-3041 (1998-09-25)
Batch data of aerobic microbial degradation rate constants Kb of phenylthio, phenylsulfinyl and phenylsulfonyl acetates have been determined, and the qualitative relationships between their Kb and chemical structures were analyzed. The phenylthio acetates were most subject to microbial transformation, followed

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