102151-52-0

Usage

Structure

Contains an imidazole ring with a hydroxymethyl group and a benzyl ether group
Derived from imidazole, a five-membered heterocyclic ring containing nitrogen
Potential applications in medicinal chemistry or drug development due to hydroxymethyl group
Aromatic and lipophilic properties from benzyl ether group
Further research needed to understand potential uses and properties of the compound

Upstream product

• 67-56-1 methanol 
• 4397-53-9 p-benzyloxybenzaldehyde 
• 96-26-4 dihydroxyacetone 

Downstream Products

• 52353-63-6 4-(hydroxymethyl)-2-(4-hydroxyphenyl)imidazole 
• 102152-23-8 2-<4-<3-<<2-(3,4-dimethoxyphenyl)ethyl>amino>-2-hydroxypropoxy>phenyl>-4-(ethoxymethyl)imidazole 
• 102281-28-7 (S)-2-<4-<3-<<2-(3,4-dimethoxyphenyl)ethyl>amino>-2-hydroxypropoxy>phenyl>-4-(methoxymethyl)imidazole 
• 102150-93-6 (S)-4-(hydroxymethyl)-2-<4-<3-<<2-(3,4-dimethoxyphenyl)ethyl>amino>-2-hydroxypropoxy>phenyl>imidazole 
• 102151-57-5 2-(4-hydroxyphenyl)-4-(methoxymethyl)imidazole 

Relevant academic research and scientific papers

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.

BETA-ADRENERGIC BLOCKING IMIDAZOLYLPHENOXY PROPANOLAMINES

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. STR1

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