CAS 4760-35-4
:2-(Chloromethyl)-1-methylbenzimidazole
Description:
2-(Chloromethyl)-1-methylbenzimidazole is an organic compound characterized by its benzimidazole core, which consists of a fused benzene and imidazole ring. The presence of a chloromethyl group at the second position and a methyl group at the first position of the benzimidazole structure contributes to its unique chemical properties. This compound typically appears as a solid and is soluble in organic solvents. It is known for its potential applications in pharmaceuticals and agrochemicals, often serving as an intermediate in the synthesis of various biologically active compounds. The chloromethyl group can participate in nucleophilic substitution reactions, making it a versatile building block in organic synthesis. Additionally, the compound may exhibit biological activity, which warrants further investigation into its pharmacological properties. As with many chemical substances, proper handling and safety precautions are essential due to potential toxicity or reactivity.
Formula:C9H9ClN2
InChI:InChI=1S/C9H9ClN2/c1-12-8-5-3-2-4-7(8)11-9(12)6-10/h2-5H,6H2,1H3
InChI key:InChIKey=WRGVPFAJPMIYOX-UHFFFAOYSA-N
SMILES:CN1C=2C(N=C1CCl)=CC=CC2
Synonyms:- 1-Methyl-2-(chloromethyl)benzimidazole
- 1H-benzimidazole, 2-(chloromethyl)-1-methyl-
- 2-(Chloromethyl)-1-methyl-1H-1,3-benzodiazole
- 2-(Chloromethyl)-1-methylbenzimidazole
- 2-(chloromethyl)-1-methyl-1H-benzo[d]imidazole
- 2-Chloromethyl-N-methylbenzimidazole
- Benzimidazole, 2-(chloromethyl)-1-methyl-
- NSC 64201
- 2-(Chloromethyl)-1-methyl-1H-benzimidazole
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Found 4 products.
2-(Chloromethyl)-1-methyl-1H-benzimidazole
CAS:Formula:C9H9ClN2Purity:98%Color and Shape:SolidMolecular weight:180.63422-Chloromethyl-1-methyl-1H-benzoimidazole
CAS:2-Chloromethyl-1-methyl-1H-benzoimidazoleFormula:C9H9ClN2Purity:≥95%Color and Shape: beige solidMolecular weight:180.63g/mol2-(Chloromethyl)-1-methyl-1H-benzimidazole hydrochloride
CAS:Controlled Product2-(Chloromethyl)-1-methyl-1H-benzimidazole hydrochloride (CMMB) is a synthetic compound that inhibits the enzyme tyrosinase, which is responsible for catalyzing the production of melanin. The tetradentate ligand in CMMB binds to the active site of tyrosinase and prevents it from catalyzing reactions. The redox potentials of CMMB make it possible to oxidize and reduce the compound, which allows for an easy synthesis. The dihedral angle between the amine and pyrimidine rings in CMMB provides a biomimetic structure that can be used to synthesize other aromatic compounds.Formula:C9H9ClN2Purity:Min. 95%Molecular weight:180.63 g/mol



