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Merck
CN

T33006

苯硫基乙酸

96%

别名:

苯基巯基乙酸, 苯硫乙酸, 苯硫代乙酸

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关于此项目

线性分子式:
C6H5SCH2COOH
化学文摘社编号:
分子量:
168.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
203-073-9
MDL number:
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产品名称

苯硫基乙酸, 96%

InChI key

MOTOSAGBNXXRRE-UHFFFAOYSA-N

InChI

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

SMILES string

OC(=O)CSc1ccccc1

assay

96%

mp

60-63 °C (lit.)

Quality Level

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pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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
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.
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)
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
Rui Zhang et al.
Bioorganic & medicinal chemistry letters, 17(14), 3855-3859 (2007-05-26)
A novel series of potent and selective PPARdelta agonists, para-alkylthiophenoxyacetic acids, was identified. The synthesis and structure-activity relationships are described.

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