53292-67-4

Basic information

• Product Name: 2-(4-methoxyphenyl)-1H-Imidazole-5-methanol
• Synonyms: 2-(4-methoxyphenyl)-1H-Imidazole-5-methanol
• CAS NO: 53292-67-4
• Molecular Weight: 204.228
• Mol File: 53292-67-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 2-(4-methoxyphenyl)-1H-Imidazole-5-methanol(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-methoxyphenyl)-1H-Imidazole-5-methanol(53292-67-4)
• EPA Substance Registry System: 2-(4-methoxyphenyl)-1H-Imidazole-5-methanol(53292-67-4)

Safety Data

• Hazardous Substances Data: 53292-67-4(Hazardous Substances Data)

Usage

Physical form

White to off-white crystalline powder

Use in pharmaceutical development

As an intermediate in the synthesis of various drugs

Therapeutic potential

Antibacterial and antifungal properties, treatment of inflammatory and autoimmune diseases

Biological significance

Inhibition of certain enzymes

Upstream product

• 67-56-1 methanol 
• 96-26-4 dihydroxyacetone 
• 123-11-5 4-methoxy-benzaldehyde 
• 874-90-8 4-methoxybenzonitrile 
• 62147-49-3 1,3-dihydroxyacetone dimer 
• 22265-37-8 4-methoxybenzamidine 

Downstream Products

• 97749-71-8 2-(4-methoxyphenyl)-1H-imidazole-4⁽⁵⁾-carbaldehyde 
• 102151-63-3 2-(4-methoxyphenyl)-4-(morpholinomethyl)imidazole 
• 97749-71-8 2-(4-Methoxy-phenyl)-3H-imidazole-4-carbaldehyde 
• 102151-64-4 2-(4-hydroxyphenyl)-4-(morpholinomethyl)imidazole 
• 102152-25-0 (S)-2-<4-<3-<<2-(3,4-dimethoxyphenyl)ethyl>amino>-2-hydroxypropoxy>phenyl>-4-(morpholinomethyl)imidazole 

Relevant articles and documents

13C CPMAS NMR as a tool for full structural description of 2-phenyl substituted imidazoles that overcomes the effects of fast tautomerization

Tautomerization of 2-phenylimidazolecarbaldehydes has not been studied in detail so far, although this process is a well-known phenomenon for imidazole derivatives. That is why we focus our study on a series of 2-phenylimidazolecarbaldehydes and their par

BETA-BLOCKING SUBSTITUTED IMIDAZOLES

Novel substituted imidazoles and methods for their preparation are disclosed. These imidazoles, and their salts, exhibit pharmacological activity which includes antihypertensive activity and β-adrenergic blocking activity.

β1-Selective Adrenoceptor Antagonists: Examples of the 2-phenyl>imidazole Class. 2

An attempt to develop a highly cardioselective β-adrenoceptor antagonist devoid of intrinsic sympathomimetic activity (ISA) focused on exploring structure-activity relationships around (S)--amino>-2-hydroxypropoxy>phen