22985-40-6

Basic information

• Product Name: α-Carbaethoxy-α-brom-β-phenyl-γ-nitro-buttersaeureaethylester
• Synonyms: α-Carbaethoxy-α-brom-β-phenyl-γ-nitro-buttersaeureaethylester
• CAS NO: 22985-40-6
• Molecular Weight: 388.215
• Mol File: 22985-40-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: α-Carbaethoxy-α-brom-β-phenyl-γ-nitro-buttersaeureaethylester(CAS DataBase Reference)
• NIST Chemistry Reference: α-Carbaethoxy-α-brom-β-phenyl-γ-nitro-buttersaeureaethylester(22985-40-6)
• EPA Substance Registry System: α-Carbaethoxy-α-brom-β-phenyl-γ-nitro-buttersaeureaethylester(22985-40-6)

Safety Data

• Hazardous Substances Data: 22985-40-6(Hazardous Substances Data)

Upstream product

• 102-96-5 (2-nitroethenyl)benzene 
• 685-87-0 Diethyl 2-bromomalonate 
• 5153-67-3 nitrostyrene 
• 71639-13-9 diethyl 2-(3-nitrophenylethyl)malonate 
• 105-53-3 diethyl malonate 

Downstream Products

• 22975-26-4 1-Phenyl-2-nitro-3.3-dicarboaethoxy-cyclopropan 
• 1382812-12-5 diethyl 2-nitro-3-phenylcyclopropane-1,1-dicarboxylate 
• 1164124-57-5 (2R,3S)-diethyl 2-nitro-3-phenylcyclopropane-1,1-dicarboxylate 

Relevant articles and documents

Enantioselective synthesis of nitrocyclopropanes via conjugate addition of bromomalonate to nitroalkenes catalyzed by Ni(II) complexes

A novel one-pot methodology for the catalytic enantioselective synthesis of highly functionalized nitrocyclopropanes promoted by chiral nickel complexes is developed. The treatment of bromomalonates with nitroalkenes under the mild reaction conditions aff