Weight | 192.001 g/mol |
---|---|
Formula | C6H3Cl2NO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
1,2-Dichloro-4-nitrobenzene (99-54-7)
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- Vibrational spectroscopic, first-order hyperpolarizability and HOMO, LUMO studies of 1,2-dichloro-4-nitrobenzene based on Hartree-Fock and DFT calculations. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2011)
- Glutathione S-aryltransferase: the effect of treating male and female rats with phenobarbitone on the apparent kinetic parameters for the conjugation of 1,2-dichloro-4-nitrobenzene and 1-chloro-2,4-dinitrobenzene with glutathione (Biochemical Journal, 1972)
- Structural determinants in domain II of human glutathione transferase M2-2 govern the characteristic activities with aminochrome, 2-cyano-1,3-dimethyl-1-nitrosoguanidine, and 1,2-dichloro-4-nitrobenzene (Protein Science, 2008)
- Characterization of phenotypes in Gstm1-null mice by cytosolic and in vivo metabolic studies using 1,2-dichloro-4-nitrobenzene. (Drug Metabolism and Disposition, 2006)
- The unique feature of dog liver cytosolic glutathione S-transferases. An isozyme not retained on the affinity column has the highest activity toward 1,2-dichloro-4-nitrobenzene. (Journal of Biological Chemistry, 1991)
- Methemoglobinemia Induced by 1,2-Dichloro-4-nitrobenzene in Mice with a Disrupted Glutathione S-Transferase Mu 1 Gene (Drug Metabolism and Disposition, 2010)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H361: Suspected of damaging fertility or the unborn child
Warning Reproductive toxicity - Category 2 - H401: Toxic to aquatic life
Hazardous to the aquatic environment, acute hazard - Category 2 -
SMILESC1=CC(=C(C=C1[N+](=O)[O-])Cl)Cl
-
InChIKeyNTBYINQTYWZXLH-UHFFFAOYSA-N
- Pubchem - 1,2-Dichloro-4-nitrobenzene
- Wikipedia - 3,4-dichloronitrobenzene
1,2-Dichloro-4-nitrobenzene is an organic compound with the formula 1,2-Cl2C6H3-4-NO2. This pale yellow solid is related to 1,2-dichlorobenzene by the replacement of one H atom with a nitro functional group. This compound is an intermediate in the synthesis of agrochemicals.
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