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Key Documents

D69807

Sigma-Aldrich

2,3-Dichlorophenol

98%

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About This Item

Fórmula linear:
Cl2C6H3OH
Número CAS:
Peso molecular:
163.00
Beilstein:
2043615
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Nível de qualidade

Ensaio

98%

forma

crystals

pb

206 °C (lit.)

pf

55-57 °C (lit.)

cadeia de caracteres SMILES

Oc1cccc(Cl)c1Cl

InChI

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

chave InChI

UMPSXRYVXUPCOS-UHFFFAOYSA-N

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Categorias relacionadas

Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Eye Irrit. 2 - Skin Irrit. 2

Código de classe de armazenamento

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

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

239.0 °F - closed cup

Ponto de fulgor (°C)

115 °C - closed cup

Equipamento de proteção individual

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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Chemosphere, 73(5), 805-812 (2008-07-22)
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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