1,3-Dichloro-2-methyl-5-nitrobenzene is an aromatic compound characterized by the presence of two chlorine atoms, a methyl group, and a nitro group attached to a benzene ring. Its molecular structure features a dichlorobenzene framework, where the chlorine substituents are located at the 1 and 3 positions, while the methyl and nitro groups are positioned at the 2 and 5 positions, respectively. This compound is typically a yellow to brown solid at room temperature and is known for its moderate solubility in organic solvents. 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. Additionally, 1,3-dichloro-2-methyl-5-nitrobenzene may pose environmental and health risks, necessitating careful handling and disposal in accordance with safety regulations. Its applications may include use in organic synthesis and as an intermediate in the production of other chemical compounds.

1,3-dichloro-2-methyl-5-nitrobenzene

1,3-DICHLORO-2-METHYL-5-NITROBENZENE

1,3-Dichloro-2-methyl-5-nitro-benzene

2,6-Dichloro-4-nitrotoluene

1,3-Dichloro-2-methyl-5-nitrobenzene is a chiral reagent used for the preparation of α-chloroamino acids. It is prepared by chlorinating 1,3-dichlorobenzene with a mixture of chlorine and methyl chloride in the presence of an acidic catalyst. This reaction yields a mixture of 2,4-dichlorobenzoic acid and 1,3-dichloro-2,5-dimethylaniline. The methyl group can be removed by catalyzed hydrogenation to give 1,3-dichloro-2-methylbenzene. The compound crystallizes from ether in needles that melt at 110°C and boils at 190°C.

CAS 7149-69-1: 1,3-dichloro-2-methyl-5-nitrobenzene

1,3-DICHLORO-2-METHYL-5-NITROBENZENE

Ref: IN-DA00FAHY

1,3-Dichloro-2-methyl-5-nitro-benzene

Ref: 10-F049482

2,6-Dichloro-4-nitrotoluene

Ref: 54-OR25607

1,3-Dichloro-2-methyl-5-nitrobenzene

Ref: 3D-FD145288