CAS 938-71-6
:4-Chloro-1-(chloromethyl)-2-nitrobenzene
Description:
4-Chloro-1-(chloromethyl)-2-nitrobenzene, with the CAS number 938-71-6, is an organic compound characterized by its aromatic structure, which includes a nitro group and two chlorinated substituents. This compound typically appears as a yellow to brown solid and is known for its moderate solubility in organic solvents such as ethanol and acetone, while being less soluble in water. The presence of both chlorine and nitro groups contributes to its reactivity, making it a useful intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its chloromethyl group can participate in nucleophilic substitution reactions, while the nitro group can undergo reduction to amines. Due to its chemical properties, it may pose certain health and environmental risks, necessitating careful handling and disposal in accordance with safety regulations. Overall, 4-Chloro-1-(chloromethyl)-2-nitrobenzene is a significant compound in synthetic organic chemistry, with applications that leverage its unique reactivity and functional groups.
Formula:C7H5Cl2NO2
InChI:InChI=1S/C7H5Cl2NO2/c8-4-5-1-2-6(9)3-7(5)10(11)12/h1-3H,4H2
InChI key:InChIKey=OMPHLGROCARZOU-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=C(CCl)C=CC(Cl)=C1
Synonyms:- 2-Nitro-4-chlorobenzyl chloride
- α,4-Dichloro-2-nitrotoluene
- Benzene, 4-chloro-1-(chloromethyl)-2-nitro-
- 4-Chloro-1-(chloromethyl)-2-nitrobenzene
- Toluene, α,4-dichloro-2-nitro-
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Found 2 products.
4-Chloro-2-nitrobenzyl chloride
CAS:Formula:C7H5Cl2NO2Purity:95%Color and Shape:LiquidMolecular weight:206.02614-Chloro-2-nitrobenzyl chloride
CAS:<p>2-Chloro-3-nitropyridine is a base that has been used in the formation of silver halides. It reacts with carbanions to form a silver bond, which can be used as a photographic emulsion. 2-Chloro-3-nitropyridine can also react with o-chloranil to form an antihelminthic drug, benzodioxole, which has been shown to be effective against the nematode Ascaris suum. 2-Chloro-3-nitropyridine is also active against bacterial and fungal infections. This drug binds to chloride or nitrobenzyl groups and forms an active agent that is useful for the treatment of these types of infections.</p>Formula:C7H5Cl2NO2Purity:Min. 95%Molecular weight:206.02 g/mol

