1023973-09-2

Basic information

• Product Name: 2-(4-bromobenzylidene)-1,3-diphenylpropane-1,3-dione
• Synonyms: 2-(4-bromobenzylidene)-1,3-diphenylpropane-1,3-dione
• CAS NO: 1023973-09-2
• Molecular Weight: 391.264
• Mol File: 1023973-09-2.mol

Chemical Properties

• CAS DataBase Reference: 2-(4-bromobenzylidene)-1,3-diphenylpropane-1,3-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-bromobenzylidene)-1,3-diphenylpropane-1,3-dione(1023973-09-2)
• EPA Substance Registry System: 2-(4-bromobenzylidene)-1,3-diphenylpropane-1,3-dione(1023973-09-2)

Safety Data

• Hazardous Substances Data: 1023973-09-2(Hazardous Substances Data)

Upstream product

• 1122-91-4 4-bromo-benzaldehyde 
• 120-46-7 1,3-diphenylpropanedione 

Downstream Products

• 1233126-02-7 (4-(4-bromophenyl)-5-(2-chlorophenyl)-2-phenylfuran-3-yl)(phenyl)methanone 
• 1233126-01-6 (4-(4-bromophenyl)-5-(4-chlorophenyl)-2-phenylfuran-3-yl)(phenyl)methanone 
• 1233126-04-9 (4-(4-bromophenyl)-5-(4-methoxyphenyl)-2-phenylfuran-3-yl)(phenyl)methanone 
• 1321201-00-6 (3R,4R)-5-benzoyl-4-(4-bromophenyl)-3-(4-fluorobenzyl)-6-phenyl-3,4-dihydro-2H-pyran-2-one 
• 1321200-99-0 (3R,4R)-5-benzoyl-3-benzyl-4-(4-bromophenyl)-6-phenyl-3,4-dihydro-2H-pyran-2-one 
• 1331773-66-0 4-benzoyl-5-(4-bromophenyl)-3-phenyl-2-oxaspiro[5.5]undec-3-en-1-one 
• 1360807-13-1 (R,E)-2-benzoyl-3-(4-bromophenyl)-6-(4-methoxyphenyl)-1-phenylhept-5-ene-1,4-dione 
• 1450988-99-4 ((2'S,3'R)-1-benzyl-3'-(4-bromophenyl)-2-oxo-5'-thioxospiro[indoline-3,2'-pyrrolidine]-4',4'-diyl)bis(phenylmethanone) 
• 1266794-15-3 (4-bromo-3-phenyloxirane-2,2-diyl)bis(phenylmethanone) 
• 1360806-99-0 (R,E)-2-benzoyl-3-(4-bromophenyl)-1-phenylhept-5-ene-1,4-dione 

Relevant articles and documents

The Regiospecific Preparation of 2-Substituted Tribenzotriquinacenes

Several substituted tribenzotriquinacene derivatives (TBTQ) carrying functional groups exclusively in the 2-position (OMe, OH, Br, CHO, CN, styryl, etc.) have been prepared by our new synthesis of the tribenzotriquinacene framework. The route has been ext

Synthesis of chiral tetrahydrofurans via catalytic asymmetric [3 + 2] cycloaddition of heterosubstituted alkenes with oxiranes

An efficient diastereo- and enantioselective [3 + 2] cycloaddition of heterosubstituted alkenes with oxiranes via selective C-C bond cleavage of epoxides has been developed. The reaction was catalyzed by a chiral N,N′-dioxide/Ni(II) catalyst, and a variety of chiral highly substituted tetrahydrofurans were obtained in up to 99% yield, 92/8 dr, and 99% ee.