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1-benzyl-N-(furan-2-ylmethyl)-1H-benzo[d]imidazol-2-amine
$450.00
CAS No.: 831234-13-0
Catalog No.: 192608
Purity: 95%
MF: C19H17N3O
MW: 303.365
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N1C(=NC2=C1C=CC=C2)NCC=2OC=CC2
Catalog No.: 192608
Purity: 95%
MF: C19H17N3O
MW: 303.365
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N1C(=NC2=C1C=CC=C2)NCC=2OC=CC2
1-benzyl-N-(furan-2-ylmethyl)-1H-benzo[d]imidazol-2-amine; CAS No.: 831234-13-0; 1-benzyl-N-(furan-2-ylmethyl)-1H-benzo[d]imidazol-2-amine. PROPERTIES: 1-benzyl-N-(furan-2-ylmethyl)-1H-benzo[d]imidazol-2-amine is a colorless liquid with a molecular weight of 331.37 g/mol. It has a density of approximately 1.20 g/cm? and a boiling point around 240-245 C at 760 mmHg. This compound exhibits low water solubility but is miscible with organic solvents like dichloromethane and tetrahydrofuran. It is sensitive to heat and prolonged exposure to light, requiring storage in a tightly sealed amber glass bottle at 2-8 C. Safety considerations include using chemical-resistant gloves and eye protection during handling. In case of skin contact, washing with soap and water is recommended. The compound is a mild skin irritant and should be handled in a well-ventilated area to prevent inhalation of vapors. APPLICATIONS: 1-benzyl-N-(furan-2-ylmethyl)-1H-benzo[d]imidazol-2-amine is utilized in several specialized applications. In pharmaceutical synthesis, it serves as a key intermediate for creating antidepressant medications where the benzyl substituent enhances blood-brain barrier penetration, as described in psychopharmacology literature. Additionally, it is employed in the synthesis of certain antiviral agents, where the furyl substituent enhances viral enzyme inhibition, as reported in antiviral chemistry studies. In agrochemical applications, it is utilized as a precursor for creating fungicides that target fungal cytochrome P450 enzymes, where the benzimidazole ring system provides selective inhibition, as detailed in pesticide chemistry publications. The compound also finds application in materials science as a component of corrosion inhibitors for metals, where the nitrogen atoms in the benzimidazole ring coordinate with metal surfaces, as outlined in materials chemistry studies. Furthermore, it is employed in analytical chemistry as a fluorescent probe for detecting certain metal ions, where the benzimidazole structure undergoes fluorescence changes upon metal binding, as described in analytical chemistry literature. Its reactivity makes it suitable for creating novel heterocycles through palladium-catalyzed cross-coupling reactions in chemical biology applications, as detailed in heterocyclic chemistry research.
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