36289-13-1

Basic information

• Product Name: 2-(2-phenyl-1H-imidazo[1,2-a]benzimidazol-1-yl)ethanol
• Synonyms: 2-(2-phenyl-1H-imidazo[1,2-a]benzimidazol-1-yl)ethanol;2-(2-phenyl-1H-imidazo[1,2-a]benzimidazol-1-yl)ethanol(SALTDATA: FREE)
• CAS NO: 36289-13-1
• Molecular Formula: C₁₇H₁₅N₃O
• Molecular Weight: 277.32
• Mol File: 36289-13-1.mol
• Article Data: 2

Chemical Properties

• Melting Point: 168-169 °C(Solv: ethyl acetate (141-78-6))
• Boiling Point: 488.9°C at 760 mmHg
• Flash Point: 249.5°C
• Appearance: /
• Density: 1.28g/cm³
• Vapor Pressure: 2.26E-10mmHg at 25°C
• Refractive Index: 1.69
• PKA: 14.73±0.10(Predicted)
• CAS DataBase Reference: 2-(2-phenyl-1H-imidazo[1,2-a]benzimidazol-1-yl)ethanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(2-phenyl-1H-imidazo[1,2-a]benzimidazol-1-yl)ethanol(36289-13-1)
• EPA Substance Registry System: 2-(2-phenyl-1H-imidazo[1,2-a]benzimidazol-1-yl)ethanol(36289-13-1)

Safety Data

• Hazardous Substances Data: 36289-13-1(Hazardous Substances Data)

Usage

Class

Organic compounds

Type

Phenylimidazoles

Structure

Aromatic heterocyclic compound with a unique benzimidazole ring structure

Usage

Mainly used in the pharmaceutical industry as a building block in the synthesis of various drugs

Properties

Exhibits potential pharmacological properties and serves as a useful tool for researchers in the development of new pharmaceuticals

Safety

Proper handling and storage procedures should be followed to ensure safety and prevent any potential hazards.

InChI:InChI=1/C17H15N3O/c21-11-10-19-16(13-6-2-1-3-7-13)12-20-15-9-5-4-8-14(15)18-17(19)20/h1-9,12,21H,10-11H2

Upstream product

• 1228647-51-5 1-(2-oxo-2-phenylethyl)benzimidazole-2-sulfonic acid 
• 141-43-5 ethanolamine 
• 154055-44-4 2-(2-hydroxyethylamino)-1-phenacylbenzimidazole 

Downstream Products

• 1241950-10-6 2-(2-bromoethylamino)-1-phenacylbenzimidazole hydrobromide 

Relevant articles and documents

1-Acylmethylbenzimidazole-2-sulfonic acids and their cyclization by N-nucleophiles

New preparation method was developed for derivatives of 1,4-dihydro-1,2,4-triazino[4,3-a]-, 2-aryl-1(9)H-, and 1-R-imidazo[1,2-a] benzimidazole underlain by newly synthesized 1-acylmethylbenzimidazole-2- sulfonic acids. The latter react with 2-aminoethanol affording along with the previously described compounds of the 1-(2-hydroxyethyl)imidazobenzimidazole series also compounds of formerly unknown polycyclic system, 2,3,11,12-tetrahydro-1,3-oxazolo[2,3-a]imidazo[1,2-a]benzimidazole.