87708-22-3

Basic information

• Product Name: 3,5-Isoxazoledicarboxylic acid, 4-(4-chlorophenyl)-4,5-dihydro-, dimethyl ester, 2-oxide
• CAS NO: 87708-22-3
• Molecular Formula: C13H12ClNO6
• Molecular Weight: 313.694
• Mol File: 87708-22-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 3,5-Isoxazoledicarboxylic acid, 4-(4-chlorophenyl)-4,5-dihydro-, dimethyl ester, 2-oxide(CAS DataBase Reference)
• NIST Chemistry Reference: 3,5-Isoxazoledicarboxylic acid, 4-(4-chlorophenyl)-4,5-dihydro-, dimethyl ester, 2-oxide(87708-22-3)
• EPA Substance Registry System: 3,5-Isoxazoledicarboxylic acid, 4-(4-chlorophenyl)-4,5-dihydro-, dimethyl ester, 2-oxide(87708-22-3)

Safety Data

• Hazardous Substances Data: 87708-22-3(Hazardous Substances Data)

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 2483-57-0 methyl 2-nitroacetate 
• 27895-56-3 [1-(4-Chloro-phenyl)-meth-(E)-ylidene]-isopropyl-amine 

Downstream Products

• 87708-26-7 methyl 6-chloro-2-methoxycarbonyl-α-(p-nitrobenzoyloxy)-1-oxido-3H-indole-3-acetate 
• 117617-32-0 (4R,5R)-4-(4-Chloro-phenyl)-4,5-dihydro-isoxazole-3,5-dicarboxylic acid dimethyl ester 

Relevant articles and documents

Highly diastereoselective condensation of α-nitro-esters with aldehydes catalyzed by zinc complexes of amino acids

Zinc complexes of amino acids efficiently catalyze the condensation between α-nitro-esters and a variety of aldehydes. An unusual domino reaction sequence leads to the diastereoselective formation of substituted isoxazoline N-oxides in high yields.