177411-39-1

Basic information

• Product Name: 2-Propenoic acid, 3-[2-(acetylamino)phenyl]-, methyl ester, (2E)-
• CAS NO: 177411-39-1
• Molecular Formula: C12H13NO3
• Molecular Weight: 219.24
• Mol File: 177411-39-1.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2-Propenoic acid, 3-[2-(acetylamino)phenyl]-, methyl ester, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 3-[2-(acetylamino)phenyl]-, methyl ester, (2E)-(177411-39-1)
• EPA Substance Registry System: 2-Propenoic acid, 3-[2-(acetylamino)phenyl]-, methyl ester, (2E)-(177411-39-1)

Safety Data

• Hazardous Substances Data: 177411-39-1(Hazardous Substances Data)

Upstream product

• 5344-90-1 2-Aminobenzyl alcohol 
• 98-95-3 nitrobenzene 
• 1795-83-1 N-Phenylacetohydroxamic acid 
• 292638-85-8 acrylic acid methyl ester 
• 615-36-1 2-bromoaniline 
• 78839-75-5 2-bromo-N-(tert-butoxycarbonyl)aniline 
• 169214-12-4 [2'-²H]acetanilide 
• 15826-91-2 acetanilide-d5 
• 103-84-4 Acetanilid 
• 1259100-79-2 N-Boc-2,N-dideuterioaniline 
• 19591-17-4 o-iodoacetanilide 
• 6213-87-2 methyl (2E)-3-bromoacrylate 
• 77-78-1 dimethyl sulfate 

Downstream Products

• 65848-66-0 4-(3-methoxyphenyl)-1H-quinolin-2-one 
• 106015-75-2 4-(4-fluorophenyl)quinolin-2(1H)-one 
• 93501-08-7 4-(4-chlorophenyl)-2-quinolinone 
• 37118-72-2 4-(p-methoxyphenyl)-2-(1H)-quinolinone 
• 106015-76-3 4-(p-tolyl)-2-(1H)-quinolinone 
• 5855-57-2 4-phenyl-2-quinolinone 
• 115984-41-3 (E)-3-[2-{(E)-2-methoxycarbonylvinyl}phenyl]acrylic acid methyl ester 
• 1373442-32-0 (E)-2-(3-methoxy-3-oxoprop-1-en-1-yl)benzene-1-diazonium tetrafluoroborate 
• 21156-62-7 N-acetylphenylalanine methyl ester 
• 59-31-4 2-hydroxyquinoline 

Relevant articles and documents

Aerobic waste-minimized Pd-catalysed C-H alkenylation in GVL using a tube-in-tube heterogeneous flow reactor

Herein we report the design and application of a tube-in-tube packed-bed flow reactor for the first time for the development of a heterogeneous palladium catalysed oxidative C-C bond formation process. In particular, we have defined an innovative tube-in-

Pd-catalyzed aerobic oxidative coupling of anilides with olefins through regioselective C-H bond activation

Pd-catalyzed aerobic oxidative coupling of anilides with olefins was achieved through selective C-H bond activation. Compared to the previous studies, not only did we successfully use molecular oxygen to replace the chemical oxidant, but we also obtained

Heterogeneous C-H alkenylations in continuous-flow: Oxidative palladium-catalysis in a biomass-derived reaction medium

Herein we report the unprecedented Fujiwara-Moritani reaction catalysed by the commercially available heterogeneous palladium catalyst Pd/C. The reaction works efficiently in GVL, a biomass derived solvent, in the coupling between variously substituted ac

Oxidative olefination of anilides with unactivated alkenes catalyzed by an (electron-deficient η5-cyclopentadienyl)rhodium(III) complex under ambient conditions

The oxidative olefination of sp2 C-H bonds of anilides with both activated and unactivated alkenes using an (electron-deficient η5-cyclopentadienyl)rhodium(III) complex is reported. In contrast to reactions using this electron-defici