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Merck
CN

540854

Sigma-Aldrich

4-异丙基苯硫酚

95%

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About This Item

线性分子式:
(CH3)2CHC6H4SH
CAS号:
分子量:
152.26
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

95%

折射率

n20/D 1.552 (lit.)

沸点

99-100 °C/14 mmHg (lit.)

密度

0.979 g/mL at 25 °C (lit.)

SMILES字符串

CC(C)c1ccc(S)cc1

InChI

1S/C9H12S/c1-7(2)8-3-5-9(10)6-4-8/h3-7,10H,1-2H3

InChI key

APDUDRFJNCIWAG-UHFFFAOYSA-N

一般描述

4-Isopropylbenzenethiol is an aromatic thiol. It undergoes oxidation in the presence of activated carbon and xylene to afford the corresponding disulfide. 4-Isopropylbenzenethiol reacts with 2-chloro-3-formylquinolines and NaH in DMSO to afford the corresponding 2-(4-isopropylphenylthio)quinoline-3-carbaldehyde.

应用

4-Isopropylbenzenethiol may be used to synthesize 4-(4-isopropyl-phenylsulfanyl)-benzene-1,2-diol.

象形图

CorrosionExclamation mark

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

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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First construction of 12H-thiochromeno [2, 3-b] quinolines and 5H-benzo [7, 8] thiocino-[2, 3-b] quinolines via intramolecular Friedel-Crafts reaction of Morita-Baylis-Hillman adducts.
Zhong W, et al.
Tetrahedron, 67(19), 3509-3518 (2011)
Oxidative transformation of thiols to disulfides promoted by activated carbon-air system.
Hayashi M, et al.
Tetrahedron Letters, 51(51), 6734-6736 (2010)
Tsuneo Kashiwagi et al.
Chemical communications (Cambridge, England), 48(22), 2806-2808 (2012-02-04)
We have successfully demonstrated that a microflow reactor is extremely useful in controlling reactions involving an unstable o-benzoquinone. The key features of the method are an effective o-benzoquinone generation and its rapid use for the following reaction without decomposition in
Homan Kang et al.
Scientific reports, 5, 10144-10144 (2015-05-29)
Recently, preparation and screening of compound libraries remain one of the most challenging tasks in drug discovery, biomarker detection, and biomolecular profiling processes. So far, several distinct encoding/decoding methods such as chemical encoding, graphical encoding, and optical encoding have been

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