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C62808

Sigma-Aldrich

3-Chlorophenol

98%

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About This Item

Formula condensata:
ClC6H4OH
Numero CAS:
108-43-0
Peso molecolare:
128.56
Beilstein:
1634401
Numero CE:
203-582-6
Numero MDL:
MFCD00002256
Codice UNSPSC:
12352100
ID PubChem:
24892854
NACRES:
NA.22

Saggio

98%

Forma fisica

solid

Indice di rifrazione

n20/D 1.563 (lit.)

P. eboll.

214 °C (lit.)

Punto di fusione

31-34 °C (lit.)

Densità

1.218 g/mL at 25 °C (lit.)

Stringa SMILE

Oc1cccc(Cl)c1

InChI

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

Informazioni sul gene

rat ... Ar(24208)

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Categorie correlate

Applicazioni

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.

Avvertenze

Danger

Indicazioni di pericolo

H302 + H312 + H332,H315,H318,H411

Classi di pericolo

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

Codice della classe di stoccaggio

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

Classe di pericolosità dell'acqua (WGK)

WGK 2

Punto d’infiammabilità (°F)

248.0 °F - closed cup

Punto d’infiammabilità (°C)

120 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves

Certificati d'analisi (COA)

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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)
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)
Neng-Chou Shang et al.
Journal of environmental science and health. Part A, Toxic/hazardous substances & environmental engineering, 37(2), 261-271 (2002-02-16)
This study investigates the variation of toxicity during ozonation of 2-chlorophenol (2-CP), 3-chlorophenol (3-CP) and 4-chlorophenol (4-CP) in neutral condition. Acute toxicity of pure chlorophenols (CPs) and their ozonated intermediates was evaluated by Microtox assay. The results revealed that the
S H Lin et al.
Waste management (New York, N.Y.), 22(6), 595-603 (2002-09-07)
Experimental investigations were conducted on the adsorption characteristics of phenol and m-chlorophenol by organobentonites. The organobentonites were prepared by modifying natural bentonite with various quaternary ammonium salts including tetramethylammonium bromide, hexadecyltrimethylammonium bromide, benzyl-triethylammonium bromide, tetraethylammonium bromide and cetylpyridinium bromide. The
Young Ku et al.
Water research, 39(6), 1093-1098 (2005-03-16)
The decomposition rates of several monochlorophenol by sonolysis were enhanced by the presence of hydrogen peroxide. An optimum concentration of hydrogen peroxide was observed for achieving maximum sonolysis rate of monochlorophenol. The decomposition rates of 3-chlorophenol by sonolysis were higher
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