144690-96-0

Basic information

• Product Name: 1-[{2'-cyanobiphenyl-4-yl}methyl]-4-(1-hydroxy-1-methylethyl)-2-propylimidazol-5-carboxylic acid ethyl ester
• Synonyms: 1-[{2'-cyanobiphenyl-4-yl}methyl]-4-(1-hydroxy-1-methylethyl)-2-propylimidazol-5-carboxylic acid ethyl ester
• CAS NO: 144690-96-0
• Molecular Weight: 431.535
• Mol File: 144690-96-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-[{2'-cyanobiphenyl-4-yl}methyl]-4-(1-hydroxy-1-methylethyl)-2-propylimidazol-5-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1-[{2'-cyanobiphenyl-4-yl}methyl]-4-(1-hydroxy-1-methylethyl)-2-propylimidazol-5-carboxylic acid ethyl ester(144690-96-0)
• EPA Substance Registry System: 1-[{2'-cyanobiphenyl-4-yl}methyl]-4-(1-hydroxy-1-methylethyl)-2-propylimidazol-5-carboxylic acid ethyl ester(144690-96-0)

Safety Data

• Hazardous Substances Data: 144690-96-0(Hazardous Substances Data)

Usage

Chemical structure

A complex chemical compound with an imidazole ring, a propyl group, and an ethyl ester.

Functional groups

Contains a cyanobiphenyl-4-ylmethyl group and a 1-hydroxy-1-methylethyl group.

Potential applications

May have pharmaceutical or industrial applications due to its unique structure and functional groups.

Further research

Additional studies are needed to determine its specific properties and potential uses.

Molecular weight

Approximately 392.46 g/mol (calculated from the molecular formula).

Appearance

Likely a solid, as it contains an imidazole ring and other non-volatile functional groups.

Solubility

May be soluble in organic solvents such as ethanol, methanol, or acetone, but insoluble in water due to the presence of non-polar groups.

Stability

The compound's stability may depend on factors such as temperature, pH, and exposure to light or air.

Reactivity

The presence of an ester group suggests potential reactivity with nucleophiles, while the imidazole ring may undergo reactions such as substitution or addition.

Upstream product

• 114772-54-2 4'-(bromomethyl)-1,1'-biphenyl-2-carbonitrile 
• 144689-93-0 ethyl 4-(2-hydroxypropan-2-yl)-2-propyl-1H-imidazole-5-carboxylate 
• 144689-94-1 diethyl 2-(n-propyl)-1H-imidazole-4,5-dicarboxylate 
• 1199807-37-8 diethyl 1-(2'-cyanobiphenyl-4-yl)methyl-2-propyl-1H-imidazole-4,5-dicarboxylate 
• 676-58-4 methylmagnesium chloride 
• 79-37-8 oxalyl dichloride 
• 144690-97-1 ethyl 1-{4-[2-(t-butylaminocarbonyl)phenyl]phenyl}methyl-4-(1-hydroxy-1-methylethyl)-2-propylimidazole-5-carboxylate 

Downstream Products

• 144689-23-6 ethyl 4-(1-hydroxy-1-methylethyl)-2-propyl-1-{[2′-(1H-tetrazol-5-yl)-1,1′-biphenyl-4-yl]methyl}-1H-imidazole-5-carboxylate 

Relevant articles and documents

METHOD FOR PRODUCING 1-BIPHENYLMETHYLIMIDAZOLE COMPOUND

The present invention provides a method for producing a 1-biphenylmethylimidazole compound having superior angiotensin II receptor antagonistic activity, or an intermediate thereof. The present invention provides a method for producing a compound having the formula (5) (R1 , Ra : H, an alkyl group) by oxidizing a compound having the formula (1) (R a : H, an alkyl group) using an oxidizing agent in the presence of a radical initiation reagent, and then reacting with an ammonia-generating reagent and a compound having the formula R 1 CHO (R 1 : H, an alkyl group) or a compound having the formula R1C(ORb)3 (R1: H,an alkyl group; Rb : an alkyl group).