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Merck
CN

184055

2-甲氧基苯硫酚

97%

别名:

2-甲氧基硫代苯酚, 硫代愈疮木酚, 邻甲氧基苯硫酚

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关于此项目

线性分子式:
CH3OC6H4SH
化学文摘社编号:
分子量:
140.20
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
230-605-7
Beilstein/REAXYS Number:
2042178
MDL number:
Assay:
97%
Form:
liquid
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产品名称

2-甲氧基苯硫酚, 97%

InChI key

DSCJETUEDFKYGN-UHFFFAOYSA-N

InChI

1S/C7H8OS/c1-8-6-4-2-3-5-7(6)9/h2-5,9H,1H3

SMILES string

COc1ccccc1S

assay

97%

form

liquid

refractive index

n20/D 1.591 (lit.)

bp

99 °C/8 mmHg (lit.)

density

1.152 g/mL at 25 °C (lit.)

Quality Level

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Application

2-Methoxythiophenol was used in the synthesis of:
  • (4S)-N-[(2S)-2-methy-3-(2-methoxyphenylthio)propanoyl]-4-phenyloxazolidin-2-one
  • 2-(4-fluorophenyl)-6-(2-methoxyphenylsulfanyl)imidazo[1,2-a]pyridine
  • 2-(2-methoxyphenylsulfanyl)benzoic acid

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

存储类别

10 - Combustible liquids

wgk

WGK 3

flash_point_f

204.8 °F - closed cup

flash_point_c

96 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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A general and efficient method for the copper-catalyzed cross-coupling of amides and thiophenols with 6-halogenoimidazo [1, 2-a] pyridines.
Enguehard-Gueiffier C, et al.
Tetrahedron, 62(25), 6042-6049 (2006)
Asymmetric conjugate addition of thiols to chiral methacryloyloxazolidinones.
Tseng T-C and Wu M-J.
Tetrahedron Asymmetry, 6(7), 1633-1640 (1995)
2-(2-Methoxyphenylsulfanyl) benzoic acid.
Li A-J, et al.
Acta Crystallographica Section E, Structure Reports Online, 62(3), o1176-o1177 (2006)
Acute toxicity of thioguaiacol and of versalide in rodents.
K R Butterworth et al.
Food and cosmetics toxicology, 19(6), 753-755 (1981-12-01)
Jennifer A Jacobsen et al.
Journal of medicinal chemistry, 54(2), 591-602 (2010-12-30)
Fragment-based lead design (FBLD) has been used to identify new metal-binding groups for metalloenzyme inhibitors. When screened at 1 mM, a chelator fragment library (CFL-1.1) of 96 compounds produced hit rates ranging from 29% to 43% for five matrix metalloproteases

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