CAS 38939-88-7
:2-Chloro-4-methyl-1-nitrobenzene
Description:
2-Chloro-4-methyl-1-nitrobenzene is an organic compound characterized by its aromatic structure, featuring a benzene ring substituted with a chlorine atom, a methyl group, and a nitro group. The chlorine atom is located at the second position, while the methyl and nitro groups are positioned at the fourth and first positions, respectively. This compound is typically a pale yellow to brown solid at room temperature and is known for its moderate solubility in organic solvents, such as ethanol and acetone, but limited solubility in water. It exhibits properties typical of nitro-substituted aromatic compounds, including potential reactivity in electrophilic substitution reactions. The presence of the nitro group contributes to its electron-withdrawing characteristics, influencing its reactivity and stability. 2-Chloro-4-methyl-1-nitrobenzene is utilized in various chemical syntheses and may serve as an intermediate in the production of dyes, pharmaceuticals, and agrochemicals. As with many chlorinated and nitro compounds, it is important to handle this substance with care due to potential toxicity and environmental concerns.
Formula:C7H6ClNO2
InChI:InChI=1S/C7H6ClNO2/c1-5-2-3-7(9(10)11)6(8)4-5/h2-4H,1H3
InChI key:InChIKey=KGSQRFPDZCBVBS-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(Cl)C=C(C)C=C1
Synonyms:- 1-Chloro-5-methyl-2-nitrobenzene
- 1-Methyl-3-chloro-4-nitrobenzene
- 2-Chloro-4-Methyl-1-Nitrobenzene
- 2-Chloro-4-methylnitrobenzene
- 5-Methyl-2-nitrochlorobenzene
- Benzene, 2-chloro-4-methyl-1-nitro-
- Toluene, 3-chloro-4-nitro-
- 3-Chloro-4-nitrotoluene
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Found 5 products.
3-Chloro-4-nitrotoluene
CAS:Formula:C7H6ClNO2Purity:>98.0%(GC)Color and Shape:White or Colorless to Orange to Green powder to lump to clear liquidMolecular weight:171.58Benzene, 2-chloro-4-methyl-1-nitro-
CAS:Formula:C7H6ClNO2Purity:98%Color and Shape:LiquidMolecular weight:171.58103-Chloro-4-nitrotoluene
CAS:<p>3-Chloro-4-nitrotoluene (3CNT) is a lactam that is produced from hydrochloric acid and styrene. 3CNT has a reactive nature, as it readily undergoes dehydration to produce benzothiazine. The reaction of 3CNT with hydroxamic acids yields the corresponding nitro compound, which can be used for the synthesis of organic compounds. 3CNT also reacts with protonated amines to form an oxazoline derivative. 3CNT is used in cross-coupling reactions, which are important for the synthesis of complex molecules such as pharmaceuticals and agrochemicals. Kinetic data on 3CNT’s reaction with hydroxamic acids show that it has a high rate of conversion to nitro compounds.</p>Formula:C7H6ClNO2Purity:Min. 95%Color and Shape:PowderMolecular weight:171.58 g/mol2-Chloro-4-methyl-1-nitrobenzene
CAS:Formula:C7H6ClNO2Purity:98%Color and Shape:SolidMolecular weight:171.58




