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Merck
CN

C62794

Sigma-Aldrich

2-氯苯酚

98%

别名:

o-Chlorophenol

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About This Item

线性分子式:
ClC6H4OH
CAS号:
分子量:
128.56
Beilstein:
1905114
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

98%

表单

liquid

折射率

n20/D 1.558 (lit.)

沸点

175-176 °C (lit.)

mp

8 °C (lit.)

密度

1.241 g/mL at 25 °C (lit.)

SMILES字符串

Oc1ccccc1Cl

InChI

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

InChI key

ISPYQTSUDJAMAB-UHFFFAOYSA-N

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应用

2-Chlorophenol is used to synthesize various organic intermediates and compounds including several polycyclic aromatic hydrocarbons and pharmacologically active molecules. It is used as a precursor to synthesize polychlorinated dibenzo p-dioxins and dibenzofurans (PCDD/Fs).

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 Corr. 1B

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)

147.2 °F - closed cup

闪点(°C)

64.0 °C - closed cup

个人防护装备

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

法规信息

危险化学品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

A quantum mechanical study on the formation of PCDD/Fs from 2-chlorophenol as precursor.
Zhang, Qingzhu et al.
Environmental Science & Technology, 42(19), 7301-7308 (2008)
Hydroxyterphenylphoshine- Palladium Catalyst for Benzo [b] furan Synthesis from 2-Chlorophenols. Bifunctional Ligand Strategy for Cross-Coupling of Chloroarenes.
Wang, Jia-Rui and Manabe, Kei
The Journal of Organic Chemistry, 75(15), 5340-5342 (2010)
Synthesis and anti-inflammatory activity evaluation of some novel 6-alkoxy (phenoxy)-[1, 2, 4] triazolo [3, 4-a] phthalazine-3-amine derivatives.
Sun, Xian-Yu et al.
European Journal of Medicinal Chemistry, 45(11), 4807-4812 (2010)
Microwave-promoted Suzuki-Miyaura coupling of arylboronic acids with 1-bromo-2-naphthol, o-bromophenol, and o-chlorophenol.
Wawrzyniak P and Heinicke J.
Tetrahedron Letters, 47(50), 8921-8924 (2006)
Thi Thu Nga Nguyen et al.
The Journal of antimicrobial chemotherapy, 70(3), 731-738 (2014-10-23)
HIV resistance to the integrase inhibitor raltegravir in treated patients is characterized by distinct resistance pathways. We hypothesize that differences in the in vivo dynamics of HIV resistance to raltegravir are due to the genetic context of the integrase present

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