959298-68-1

Basic information

• Product Name: (E)-methyl 3-(2-(benzylamino)phenyl)-acrylate
• Synonyms: (E)-methyl 3-(2-(benzylamino)phenyl)-acrylate
• CAS NO: 959298-68-1
• Molecular Weight: 267.327
• Mol File: 959298-68-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (E)-methyl 3-(2-(benzylamino)phenyl)-acrylate(CAS DataBase Reference)
• NIST Chemistry Reference: (E)-methyl 3-(2-(benzylamino)phenyl)-acrylate(959298-68-1)
• EPA Substance Registry System: (E)-methyl 3-(2-(benzylamino)phenyl)-acrylate(959298-68-1)

Safety Data

• Hazardous Substances Data: 959298-68-1(Hazardous Substances Data)

Upstream product

• 615-36-1 2-bromoaniline 
• 76464-99-8 N-benzyl-2-iodoaniline 
• 292638-85-8 acrylic acid methyl ester 
• 71687-81-5 N-benzyl-2-bromoaniline 

Downstream Products

• 697759-12-9 N-benzyl-4-phenyl-1,2,3,4-tetrahydroquinolin-2-one 
• 1224738-73-1 C₂₃H₂₃NO₂ 
• 1224738-26-4 N-benzyl-3,4-dihydro-4-(4-hydroxyphenyl)quinolin-2(1H)-one 
• 1224738-24-2 N-benzyl-3,4-dihydro-4-(4-methoxyphenyl)quinolin-2(1H)-one 
• 1224738-20-8 N-benzyl-3,4-dihydro-4-p-tolylquinolin-2(1H)-one 
• 1224738-32-2 N-benzyl-3,4-dihydro-4-(4-fluorophenyl)quinolin-2(1H)-one 
• 1224738-34-4 N-benzyl-4-(4-chlorophenyl)-3,4-dihydroquinolin-2(1H)-one 
• 1224738-36-6 N-benzyl-4-(3-chlorophenyl)-3,4-dihydroquinolin-2(1H)-one 
• 1224738-22-0 N-benzyl-3,4-dihydro-4-(3-methoxyphenyl)quinolin-2(1H)-one 
• 1224738-28-6 N-benzyl-3,4-dihydro-4-(2-naphthyl)quinolin-2(1H)-one 
• 1224738-30-0 N-benzyl-3,4-dihydro-4-(3-nitrophenyl)quinolin-2(1H)-one 
• 1224738-38-8 N-benzyl-4-(4-acetylphenyl)-3,4-dihydroquinolin-2(1H)-one 

Relevant articles and documents

ALPHA-CINNAMIDE COMPOUNDS AND COMPOSITIONS AS HDAC8 INHIBITORS

The present invention relates to inhibitors of histone deacetylases, in particular HDAC8, that are useful for the treatment of cancer and other diseases and disorders, as well as the synthesis and applications of said inhibitors.

Rhodium-catalyzed domino conjugate addition-cyclization reactions for the synthesis of a variety of N- and O-heterocycles: Arylboroxines as effective carbon nucleophiles

Facile and efficient Rh(I)-catalyzed domino conjugate addition-cyclization reactions of olefins bearing two electrophilic sites and a pendant nucleophile with organoboroxines have been developed to afford a variety of N- and O-heterocycles, such as 3,4-dihydroquinolin-2(1H)-ones, 3,4-dihydrocoumarins, and pyrrolidin-2-ones, which constitute important motifs in biologically active natural and synthetic organic compounds.