1255772-74-7

Basic information

• Product Name: 1-benzyl-3-phenyl-3,4-dihydroquinoxalin-2(1H)-one
• Synonyms: 1-benzyl-3-phenyl-3,4-dihydroquinoxalin-2(1H)-one
• CAS NO: 1255772-74-7
• Molecular Weight: 314.387
• Mol File: 1255772-74-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 1-benzyl-3-phenyl-3,4-dihydroquinoxalin-2(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-3-phenyl-3,4-dihydroquinoxalin-2(1H)-one(1255772-74-7)
• EPA Substance Registry System: 1-benzyl-3-phenyl-3,4-dihydroquinoxalin-2(1H)-one(1255772-74-7)

Safety Data

• Hazardous Substances Data: 1255772-74-7(Hazardous Substances Data)

Upstream product

• 95-54-5 1,2-diamino-benzene 
• 1504-78-5 3-phenylquinoxaline-2(1H)-one 
• 1603-79-8 phenylglyoxylic acid ethyl ester 

Relevant articles and documents

Biomimetic reduction of imines and heteroaromatics with chiral and regenerable [2.2]Paracyclophane-Based NAD(P)H model CYNAM

In our previous work, we reported the synthesis of chiral and regenerable [2.2]paracyclophane-derived NAD(P)H models CYNAMs and their application in biomimetic asymmetric reduction of tetrasubstituted olefins. Herein, the biomimetic asymmetric reduction o

4,5-Dihydropyrrolo[1,2-a]quinoxalines: A tunable and regenerable biomimetic hydrogen source

A series of tunable and regenerable biomimetic hydrogen sources, 4,5-dihydropyrrolo[1,2-a]quinoxalines, have been synthesized and applied in biomimetic asymmetric hydrogenation of 3-aryl-2H-benzo[b][1,4]oxazines and 1-alkyl-3-aryl-quinoxalin-2(1H)-ones, providing the chiral amines with up to 92% and 89% ee, respectively.

The first general, highly enantioselective lewis base organocatalyzed hydrosilylation of benzoxazinones and quinoxalinones

The first general, highly enantioselective hydrosilylation of benzoxazinones and quinoxalinones has been developed. The chiral Lewis base organocatalysis that are readily accessible from (1S,2R)-ephedrine and (1R,2S)-ephedrine promoted the title reaction to afford various chiral dihydrobenzoxazinones and dihydroquinoxalinones with good yields as well as good enantioselectivities.