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Merck
CN

W421001

Sigma-Aldrich

硫代醋酸

96%

别名:

硫代乙酸

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关于此项目

线性分子式:
CH3COSH
化学文摘社编号:
分子量:
76.12
FEMA编号:
4210
Beilstein:
1733298
EC 号:
MDL编号:
UNSPSC代码:
12164502
PubChem化学物质编号:
Flavis编号:
12.199
NACRES:
NA.21
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生物来源

synthetic

质量水平

方案

96%

折射率

n20/D 1.465 (lit.)

沸点

88-91.5 °C (lit.)

密度

1.065 g/mL at 25 °C (lit.)

应用

flavors and fragrances

文件

see Safety & Documentation for available documents

食品过敏原

no known allergens

性状检查

meaty; roasted

SMILES字符串

CC(S)=O

InChI

1S/C2H4OS/c1-2(3)4/h1H3,(H,3,4)

InChI key

DUYAAUVXQSMXQP-UHFFFAOYSA-N

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免责声明

For R&D or non-EU Food use. Not for retail sale.

警示用语:

Danger

危险分类

Acute Tox. 3 Oral - Acute Tox. 4 Inhalation - Eye Dam. 1 - Flam. Liq. 2 - Skin Sens. 1

储存分类代码

3 - Flammable liquids

WGK

WGK 3

闪点(°F)

64.4 °F - closed cup

闪点(°C)

18 °C - closed cup

个人防护装备

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

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Md Ashraful Hoque et al.
Bioorganic & medicinal chemistry letters, 22(21), 6770-6772 (2012-10-02)
Two thioacetate tails were introduced to the chlamydocin- and CHAP31-related cyclic tetrapeptides. An intramolecular disulfide bridge could be formed in the CHAP31-related cyclic peptides. Both the thioacetate-tailed and disulfide-bridged peptides were potent histone deacetylase inhibitors in the presence of sulfhydryl
Brian C Smith et al.
Biochemistry, 46(50), 14478-14486 (2007-11-22)
Sir2 protein deacetylases (or sirtuins) catalyze NAD+-dependent conversion of epsilon-amino-acetylated lysine residues to deacetylated lysine, nicotinamide, and 2'-O-acetyl-ADP-ribose. Small-molecule modulation of sirtuin activity might treat age-associated diseases, such as type II diabetes, obesity, and neurodegenerative disorders. Here, we have evaluated
Ning Shangguan et al.
Journal of the American Chemical Society, 125(26), 7754-7755 (2003-06-26)
A new amide synthesis strategy based on a fundamental mechanistic revision of the reaction of thio acids and organic azides is presented. The data demonstrate that amines are not formed as intermediates in this reaction. Alternative mechanisms proceeding through a
Krista M Wager et al.
Organic letters, 13(15), 4052-4055 (2011-07-07)
A method for preparing benzyl aryl thioethers utilizing an in situ deprotection of benzyl thioacetates as an alternative to free thiols as starting materials has been developed and optimized. Good to excellent yields of diverse benzyl aryl thioethers are obtained
Christina Wedemeyer-Exl et al.
Organic & biomolecular chemistry, 5(13), 2119-2128 (2007-06-22)
The thiol-dependent methylation of heptamethyl cob(II)yrinate 8r with methyl iodide and methyl tosylate was explored under a variety of conditions. The interaction of the heptamethyl cob(II)yrinate with a variety of thiols was monitored prior to the addition of the methylating

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