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D69807

Sigma-Aldrich

2,3-Dichlorophenol

98%

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About This Item

Formula condensata:
Cl2C6H3OH
Numero CAS:
Peso molecolare:
163.00
Beilstein:
2043615
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22

Livello qualitativo

Saggio

98%

Stato

crystals

P. ebollizione

206 °C (lit.)

Punto di fusione

55-57 °C (lit.)

Stringa SMILE

Oc1cccc(Cl)c1Cl

InChI

1S/C6H4Cl2O/c7-4-2-1-3-5(9)6(4)8/h1-3,9H
UMPSXRYVXUPCOS-UHFFFAOYSA-N

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Categorie correlate

Pittogrammi

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Avvertenze

Warning

Indicazioni di pericolo

Classi di pericolo

Eye Irrit. 2 - 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 3

Punto d’infiammabilità (°F)

239.0 °F - closed cup

Punto d’infiammabilità (°C)

115 °C - closed cup

Dispositivi di protezione individuale

dust mask type N95 (US), Eyeshields, Gloves


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Reductive dehalogenase (RD) gene transcript levels in Dehalococcoides ethenogenes strain 195 were investigated using reverse transcriptase quantitative PCR during growth and reductive dechlorination of tetrachloroethene (PCE), trichloroethene (TCE), or 2,3-dichlorophenol (2,3-DCP). Cells grown with PCE or TCE had high transcript
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In this study titanium dioxide nanotube (TNT) arrays were prepared by an anodic oxidation process with post-calcination. The morphology and structure of the TNT films were studied by field-emission scanning electron microscopy (FESEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy
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In this study, the highly-ordered TiO(2) nanotube (TNT) arrays on titanium sheets were prepared by an anodic oxidation method. Under UV illumination, the TNT films demonstrated the higher photocatalytic activity in terms of 2,3-dichlorophenol (2,3-DCP) degradation in aqueous solution than
S Goenechea et al.
Archiv der Pharmazie, 334(3), 101-103 (2001-04-24)
The beta-D-glucuronides of 2,3-, 3,4-, and 2,6-dichlorophenol (1-3) were prepared by a modified Koenigs-Knorr synthesis. As the alkaline hydrolysis of perpivaloylated methyl (2,3-dichlorophenyl)-glucuronate 1a led to a dehydrated glucuronide, the preparation of peracetylated methyl dichlorophenylglucuronates with subsequent cleavage of the

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