CAS 451485-67-9

4-(1H-Benzimidazol-1-yl)benzenemethanol

Description:

4-(1H-Benzimidazol-1-yl)benzenemethanol, identified by its CAS number 451485-67-9, is an organic compound characterized by the presence of a benzimidazole moiety and a benzyl alcohol functional group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, including stability and potential for hydrogen bonding due to the hydroxyl (-OH) group. The benzimidazole ring contributes to its biological activity, often associated with various pharmacological effects, such as antimicrobial or anticancer properties. The compound is likely to be soluble in polar solvents due to the hydroxyl group, while its aromatic structure may confer some degree of lipophilicity. Its molecular structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry. Additionally, the presence of both the benzimidazole and benzyl alcohol functionalities may facilitate further chemical modifications, enhancing its utility in drug design and development. Overall, this compound represents a versatile scaffold in organic synthesis and medicinal applications.

Formula: C₁₄H₁₂N₂O

InChI: InChI=1S/C14H12N2O/c17-9-11-5-7-12(8-6-11)16-10-15-13-3-1-2-4-14(13)16/h1-8,10,17H,9H2

InChI key: InChIKey=IRZKUEWQJPIBJF-UHFFFAOYSA-N

SMILES: C(O)C1=CC=C(N2C=3C(N=C2)=CC=CC3)C=C1

Synonyms:

• Benzenemethanol, 4-(1H-benzimidazol-1-yl)-
• [4-(Benzimidazol-1-yl)phenyl]methanol
• [4-(1H-1,3-Benzodiazol-1-yl)phenyl]methanol
• 4-(1H-Benzimidazol-1-yl)benzenemethanol

[4-(1H-1,3-Benzodiazol-1-yl)phenyl]methanol

CAS: 451485-67-9

[4-(1H-1,3-Benzodiazol-1-yl)phenyl]methanol

Purity: 95%

Molecular weight: 224.26g/mol

Ref: 54-OR32677

[4-(1H-1,3-Benzodiazol-1-yl)phenyl]methanol

CAS: 451485-67-9

4-(1H-1,3-benzodiazol-1-yl)phenylmethanol is a sesquiterpene lactone that has been shown to have antioxidant and anti-inflammatory activities. It also has a role in the coordination geometry of metal ions. 4-(1H-1,3-Benzodiazol-1-yl)phenylmethanol has been found to be an effective treatment for autoimmune diseases and cervical cancer. The molecule also inhibits the growth of bacteria by binding to cell membranes with high affinity. This causes changes in the permeability of membranes, which leads to cell death by disrupting cellular homeostasis. In addition, 4-(1H-1,3-Benzodiazol-1-yl)phenylmethanol has synergistic effects with other antimicrobial agents and may be useful in combination therapy against cancer cells.

Formula: C₁₄H₁₂N₂O

Purity: Min. 95%

Molecular weight: 224.26 g/mol

Ref: 3D-BTA48567