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Documentos Principais

D68800

Sigma-Aldrich

1,2-Dichloro-4-nitrobenzene

99%

Sinônimo(s):

3,4-Dichloronitrobenzene, asym.-Nitro-o-dichlorobenzene

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About This Item

Fórmula linear:
Cl2C6H3NO2
Número CAS:
Peso molecular:
192.00
Beilstein:
1818163
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Nível de qualidade

Ensaio

99%

forma

crystals

pb

255-256 °C (lit.)

pf

39-41 °C (lit.)

cadeia de caracteres SMILES

[O-][N+](=O)c1ccc(Cl)c(Cl)c1

InChI

1S/C6H3Cl2NO2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H

chave InChI

NTBYINQTYWZXLH-UHFFFAOYSA-N

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Pictogramas

Exclamation mark

Palavra indicadora

Warning

Frases de perigo

Classificações de perigo

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Sens. 1

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

255.2 °F - closed cup

Ponto de fulgor (°C)

124 °C - closed cup

Equipamento de proteção individual

dust mask type N95 (US), Eyeshields, Faceshields, Gloves


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Visite a Biblioteca de Documentos

V Krishnakumar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 86, 196-204 (2011-11-23)
The vibrational spectra of 1,2-dichloro-4-nitrobenzene (DCNB) and 2,3,5,6-tetrachloro-1-nitrobenzene (TCNB) were computed using B3LYP methodology with 6-31G* basis set. The solid phase FTIR and FT-Raman spectra were recorded in the region 4000-400 cm(-1) and 4000-50 cm(-1), respectively. A similarity was achieved
Susila Sivapathasundaram et al.
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP, 134(1), 169-173 (2003-01-14)
The ability of cattle and deer liver to catalyse xenobiotic conjugation reactions was investigated and compared with that of the rat. Marked differences in the activity of these enzymes were noted between the domestic animals and rats. Hepatic microsomal epoxide
L O Hansson et al.
Protein science : a publication of the Protein Society, 8(12), 2742-2750 (2000-01-13)
Two human Mu class glutathione transferases, hGST M1-1 and hGST M2-2, with high sequence identity (84%) exhibit a 100-fold difference in activities with the substrates aminochrome, 2-cyano-1,3-dimethyl-1-nitrosoguanidine (cyanoDMNG), and 1,2-dichloro-4-nitrobenzene (DCNB), hGST M2-2 being more efficient. A sequence alignment with
Toshiyuki Watanabe et al.
Archives of toxicology, 80(5), 250-257 (2005-10-21)
We have reported the existence of low glutathione S-transferase (GST) dogs whose GST activity to 1,2-dichloro-4-nitrobenzene (DCNB) as a substrate (GST-D activity) is quite low, and have also reported significant individual differences in dog liver GST-D activity. The dogs were
V A Catania et al.
Life sciences, 68(4), 467-474 (2001-02-24)
Gender-related differences and the regulation by testosterone of glutathione S-transferase were studied in rat jejunum. We analyzed enzyme activity and the relative content of GST subunits. Four experimental groups of adult rats were studied: normal males, castrated males, castrated males

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