Merck
CN

109525

Sigma-Aldrich

4-甲氧基苯硫酚

97%

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别名:
4-甲氧基硫代苯酚, 对甲氧基苯硫酚
线性分子式:
CH3OC6H4SH
CAS号:
分子量:
140.20
Beilstein:
1446910
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

折射率

n20/D 1.5831 (lit.)

bp

100-103 °C/13 mmHg (lit.)

密度

1.14 g/mL at 25 °C (lit.)

SMILES string

COc1ccc(S)cc1

InChI

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

InChI key

NIFAOMSJMGEFTQ-UHFFFAOYSA-N

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应用

4-甲氧基苯硫酚被用于制备自组装单层(SAM's)表征样品,并研究SAM对n和p通道有机薄膜晶体管的影响。4-甲氧基苯硫酚被用于氟化铯-硅藻土催化的硫醚和硫酯制备

象形图

Exclamation mark

警示用语:

Warning

危险分类

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

靶器官

Respiratory system

储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

204.8 °F - closed cup

闪点(°C)

96 °C - closed cup

个人防护装备

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


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CsF-celite, an efficient solid state reagent for the syntheses of thioesters and thioethers.
Shah STA, et al.
Monatshefte fur Chemie / Chemical Monthly, 136(9), 1583-1589 (2005)
Modification of gold source and drain electrodes by self-assembled monolayer in staggered n-and p-channel organic thin film transistors.
Boudinet D, et al.
Organic Electronics, 11(2), 227-237 (2010)
Hadeel T Al-Sinjilawi et al.
Archiv der Pharmazie, 347(11), 861-872 (2014-09-16)
A series of substituted 4-oxopyrido[2,3-a]phenothiazine-3-carboxylic acids (6a-d) were prepared via cyclization of the corresponding ethyl 7-(arylthioxy)-8-nitro(or azido)-4-oxoquinoline-3-carboxylates (3a-d/4a-d), followed by hydrolysis of the resultant esters (5a-d). Among these tetracyclics, compound 6a with unsubstituted terminal benzo-ring D was the most active
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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While Markovnikov alkene reactivity is very well developed and utilized commonly in the synthesis of commodity and research chemicals, catalytic access to the anti-Markovnikov-selective adducts is a much less-developed endeavor.

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