Merck
CN

C62808

Sigma-Aldrich

3-氯苯酚

98%

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线性分子式:
ClC6H4OH
CAS号:
分子量:
128.56
Beilstein:
1634401
EC 号:
MDL编号:
PubChem化学物质编号:
NACRES:
NA.22

检测方案

98%

形式

solid

折射率

n20/D 1.563 (lit.)

bp

214 °C (lit.)

mp

31-34 °C (lit.)

密度

1.218 g/mL at 25 °C (lit.)

SMILES string

Oc1cccc(Cl)c1

InChI

1S/C6H5ClO/c7-5-2-1-3-6(8)4-5/h1-4,8H

InChI key

HORNXRXVQWOLPJ-UHFFFAOYSA-N

Gene Information

rat ... Ar(24208)

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应用

3-氯苯酚通常用于构建各种多环芳族体系。它也用于在合成有机化学中,通过钯催化的偶联反应合成芳基中间体。

警示用语:

Danger

危险分类

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Irrit. 2

储存分类代码

6.1C - Combustible, acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 2

闪点(°F)

248.0 °F - closed cup

闪点(°C)

120 °C - closed cup

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

危险化学品

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Synthesis of (+)?Antroquinonol and Analogues by Using Enantioselective Michael Reactions of Benzoquinone Monoketals.
Hsu C S and Fang J M
European Journal of Organic Chemistry, 2016(22), 3809-3816 (2016)
A Highly Versatile Catalyst System for the Cross?Coupling of Aryl Chlorides and Amines.
Lundgren R J, et al.
Chemistry?A European Journal , 16(6), 1983-1991 (2010)
Stefano M Marino et al.
Archives of biochemistry and biophysics, 505(1), 67-74 (2010-09-30)
Tyrosinase (Ty) is a copper-containing enzyme ubiquitously distributed in nature. In recent years, Ty has attracted interest as a potential detoxifying agent for xenobiotic compounds with phenolic structure. Among these, chlorophenols are particularly relevant pollutants, commonly found in waste waters.
Clarissa A Olivati et al.
Bioprocess and biosystems engineering, 32(1), 41-46 (2008-04-15)
Langmuir-Blodgett (LB) and layer-by-layer films (LbL) of a PPV (p-phenylenevinylene) derivative, an azo compound and tetrasulfonated phthalocyanines were successfully employed as transducers in an "electronic tongue" system for detecting trace levels of phenolic compounds in water. The choice of the
Catalytic direct arylation with aryl chlorides, bromides, and iodides: intramolecular studies leading to new intermolecular reactions.
Campeau LC, et al.
Journal of the American Chemical Society, 128(2), 581-590 (2006)

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