C62794
2-氯苯酚
98%
别名:
o-Chlorophenol
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关于此项目
线性分子式:
ClC6H4OH
化学文摘社编号:
分子量:
128.56
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
202-433-2
Beilstein/REAXYS Number:
1905114
MDL number:
Assay:
98%
Form:
liquid
InChI key
ISPYQTSUDJAMAB-UHFFFAOYSA-N
InChI
1S/C6H5ClO/c7-5-3-1-2-4-6(5)8/h1-4,8H
SMILES string
Oc1ccccc1Cl
assay
98%
form
liquid
refractive index
n20/D 1.558 (lit.)
bp
175-176 °C (lit.)
mp
8 °C (lit.)
density
1.241 g/mL at 25 °C (lit.)
Quality Level
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Application
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).
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - Eye Dam. 1 - Skin Corr. 1B
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 2
flash_point_f
147.2 °F - closed cup
flash_point_c
64.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
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)
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)
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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