CAS 1484-39-5

2-METHYL-1-PHENYL-1H-BENZOIMIDAZOLE

Description:

2-Methyl-1-phenyl-1H-benzimidazole, with the CAS number 1484-39-5, is an organic compound characterized by its fused benzene and imidazole rings, which contribute to its aromatic properties. This compound typically appears as a crystalline solid and is known for its potential applications in various fields, including pharmaceuticals and materials science. The presence of the methyl and phenyl groups enhances its chemical reactivity and solubility in organic solvents. It exhibits moderate stability under standard conditions but may undergo reactions typical of imidazole derivatives, such as nucleophilic substitutions or electrophilic additions. Additionally, its structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry. The compound's properties, such as melting point, boiling point, and solubility, can vary based on purity and environmental conditions. Overall, 2-methyl-1-phenyl-1H-benzimidazole is a versatile compound with significant implications in research and industry.

Formula: C₁₄H₁₂N₂

1H-Benzimidazole, 2-methyl-1-phenyl-

CAS: 1484-39-5

Formula: C₁₄H₁₂N₂

Purity: 98%

Molecular weight: 208.2585

Ref: IN-DA001KWR

2-Methyl-1-phenyl-1h-1,3-benzodiazole

CAS: 1484-39-5

Purity: 98%

Molecular weight: 208.26400756835938

Ref: 10-F656135

2-Methyl-1-phenyl-1H-1,3-benzodiazole

CAS: 1484-39-5

2-Methyl-1-phenyl-1H-1,3-benzodiazole is a quinoline and cyanine dye that contains an organometallic group. It has substituents on the nitrogen atom and heterocyclic groups in the benzimidazole and benzothiazole rings. 2-Methyl-1-phenyl-1H-1,3-benzodiazole is used as a reagent in organic synthesis reactions. It also reacts with alkyl groups to form substituted 2,2′:6′,2″ -terpyridine compounds.

Formula: C₁₄H₁₂N₂

Purity: Min. 95%

Molecular weight: 208.26 g/mol

Ref: 3D-BAA48439