T33006
(Phenylthio)acetic acid
96%
Synonym(s):
(Phenylmercapto)acetic acid, S-Phenylthioglycolic acid, Thiophenoxyacetic acid
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About This Item
Linear Formula:
C6H5SCH2COOH
CAS Number:
Molecular Weight:
168.21
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
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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signalword
Warning
hcodes
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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