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C62808

Sigma-Aldrich

3-Chlorophenol

98%

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About This Item

Fórmula lineal:
ClC6H4OH
Número de CAS:
108-43-0
Peso molecular:
128.56
Beilstein/REAXYS Number:
1634401
EC Number:
203-582-6
MDL number:
MFCD00002256
UNSPSC Code:
12352100
PubChem Substance ID:
24892854
NACRES:
NA.22

assay

98%

form

solid

refractive index

n20/D 1.563 (lit.)

bp

214 °C (lit.)

mp

31-34 °C (lit.)

density

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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Categorías relacionadas

Application

3-Chlorophenol is generally used in building various polycyclic aromatic systems. It is also employed in palladium-catalyzed coupling reactions to synthesize aryl intermediates in synthetic organic chemistry.

signalword

Danger

Hazard Classifications

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

Storage Class

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

wgk_germany

WGK 2

flash_point_f

248.0 °F - closed cup

flash_point_c

120 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves

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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)
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)
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.
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