133485-97-9

Basic information

• Product Name: (E)-3-[2-n-Butyl-1-{(2-chlorophenyl)methyl}-1H-imidazol-5-yl]-2-{1-(thien-2-yl)pentyl}-2-propenoic Acid
• Synonyms: (E)-3-[2-n-Butyl-1-{(2-chlorophenyl)methyl}-1H-imidazol-5-yl]-2-{1-(thien-2-yl)pentyl}-2-propenoic Acid
• CAS NO: 133485-97-9
• Molecular Weight: 471.063
• Mol File: 133485-97-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (E)-3-[2-n-Butyl-1-{(2-chlorophenyl)methyl}-1H-imidazol-5-yl]-2-{1-(thien-2-yl)pentyl}-2-propenoic Acid(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-3-[2-n-Butyl-1-{(2-chlorophenyl)methyl}-1H-imidazol-5-yl]-2-{1-(thien-2-yl)pentyl}-2-propenoic Acid(133485-97-9)
• EPA Substance Registry System: (E)-3-[2-n-Butyl-1-{(2-chlorophenyl)methyl}-1H-imidazol-5-yl]-2-{1-(thien-2-yl)pentyl}-2-propenoic Acid(133485-97-9)

Safety Data

• Hazardous Substances Data: 133485-97-9(Hazardous Substances Data)

Upstream product

• 1027567-73-2 2-{[2-Butyl-3-(2-chloro-benzyl)-3H-imidazol-4-yl]-hydroxy-methyl}-3-thiophen-2-yl-heptanoic acid methyl ester 
• 133486-42-7 2-n-butyl-5-(acetoxymethyl)-1-<(2-chlorophenyl)methyl>imidazole 
• 133485-55-9 2-n-butyl-1-(2-chlorophenyl)-methyl-5-hydroxymethyl-1H-imidazole 
• 133485-56-0 2-n-butyl-1-(2-chlorophenyl)methyl-1H-imidazole-5-carboxaldehyde 
• 133486-41-6 1-acetyl-4-acetoxymethyl-2-n-butylimidazole 
• 133486-66-5 methyl 3-(2-thienyl)heptanoate 
• 68283-19-2 2-n-butyl-4-(hydroxymethyl)imidazole 
• 57502-38-2 methyl (E)-3-(2-thienyl)propenoate 
• 1124-65-8 3-(2-thienyl)-2-propenoic acid 
• 17849-38-6 2-Chlorobenzyl alcohol 
• 1026273-52-8 2-[1-[2-Butyl-3-(2-chloro-benzyl)-3H-imidazol-4-yl]-meth-(E)-ylidene]-3-thiophen-2-yl-heptanoic acid methyl ester 

Relevant articles and documents

Imidazolyl-alkenoic acids useful as angiotensin II receptor antagonists

Angiotensin II receptor antagonists having the formula: STR1 which are useful in regulating hypertension and in the treatment of congestive heart failure, renal failure, and glaucoma, pharmaceutical compositions including these antagonists, and methods of using these compounds to produce angiotensin II receptor antagonism in mammals.