3156-25-0

Basic information

• Product Name: 2-[(4-METHYLPHENOXY)METHYL]-1H-BENZIMIDAZOLE
• Synonyms: IFLAB-BB F1115-0052;2-[(4-METHYLPHENOXY)METHYL]-1H-BENZIMIDAZOLE;2-P-TOLYLOXYMETHYL-1H-BENZOIMIDAZOLE
• CAS NO: 3156-25-0
• Molecular Formula: C₁₅H₁₄N₂O
• Molecular Weight: 238.28
• Mol File: 3156-25-0.mol
• Article Data: 4

Chemical Properties

• Melting Point: 148 °C
• Boiling Point: 479.3±28.0 °C(Predicted)
• Appearance: /
• Density: 1 +-.0.06 g/cm3(Predicted)
• PKA: 11.41±0.10(Predicted)
• CAS DataBase Reference: 2-[(4-METHYLPHENOXY)METHYL]-1H-BENZIMIDAZOLE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[(4-METHYLPHENOXY)METHYL]-1H-BENZIMIDAZOLE(3156-25-0)
• EPA Substance Registry System: 2-[(4-METHYLPHENOXY)METHYL]-1H-BENZIMIDAZOLE(3156-25-0)

Safety Data

• Hazardous Substances Data: 3156-25-0(Hazardous Substances Data)

Usage

Chemical Class

Benzimidazole

Physical Form

White to off-white powder

+ Anti-parasitic

Efficacy against various parasites including protozoa, helminths, and ectoparasites.

+ Potential Anti-cancer

Investigated for its potential anti-cancer properties.

+ Anti-inflammatory

Being studied for its potential anti-inflammatory properties.

+ Neurological Disorders

Shown promise as a potential treatment for neurological disorders and other diseases.

Uses

+ Research
+ Veterinary Medicine

Potential Therapeutic Applications

Being actively studied.

Upstream product

• 940-64-7 2-(4-methylphenoxy)acetic acid 
• 95-54-5 1,2-diamino-benzene 

Downstream Products

• 1258865-49-4 C₁₈H₁₇N₃O 

Relevant articles and documents

1-ethyl gallate-2-substituted phenoxymethyl benzimidazoles: Synthesis, molecular structure, antimicrobial activities and complex with Cr(III)

Summary: The design of gallate and benzimidazole containing derivatives is expected to produce new bioactive molecules with multiple applications. Here the synthesis of eight novel benzimidazole compounds containing ethyl gallate and substituted phenoxyme

Aza-Michael addition of acrylonitrile with 2-aryloxymethylbenzimidazole derivatives under microwave irradiation

A simple, rapid, and highly efficient method has been developed for the aza-Michael addition of acrylonitrile to 2-aryl-oxymethylbenzimidazole derivatives in the presence of anhydrous potassium carbonate under microwave irradiation. A series novel of 1-cyanoethyl-2-aryloxymethylbenzimidazole derivatives have been prepared and characterised by 1H NMR, 13C NMR, IR spectra and elemental analysis.