1287795-39-4

Basic information

• Product Name: (R)-2-(3-chlorophenyl)-1,2,3,4-tetrahydroquinoxaline
• Synonyms: (R)-2-(3-chlorophenyl)-1,2,3,4-tetrahydroquinoxaline
• CAS NO: 1287795-39-4
• Molecular Weight: 244.724
• Mol File: 1287795-39-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (R)-2-(3-chlorophenyl)-1,2,3,4-tetrahydroquinoxaline(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-2-(3-chlorophenyl)-1,2,3,4-tetrahydroquinoxaline(1287795-39-4)
• EPA Substance Registry System: (R)-2-(3-chlorophenyl)-1,2,3,4-tetrahydroquinoxaline(1287795-39-4)

Safety Data

• Hazardous Substances Data: 1287795-39-4(Hazardous Substances Data)

Upstream product

• 177288-16-3 C₈H₇ClO₃ 
• 95-54-5 1,2-diamino-benzene 
• 27993-83-5 2-(3-chlorophenyl)quinoxaline 

Relevant articles and documents

Asymmetric organocatalytic tandem cyclization/transfer hydrogenation: A synthetic strategy for enantioenriched nitrogen heterocycles

An asymmetric organocatalytic tandem reaction comprising cyclization/transfer hydrogenation has been established in a compatible and synergistic way, leading to the step-economical synthesis of enantioenriched tetrahydroquinoxalines and dihydroquinoxalinones from readily accessible materials in excellent enantioselectivity of up to >99% ee. This protocol of a one-operation tandem reaction combines the merits of both tandem reactions and asymmetric organocatalysis, providing an efficient strategy for concisely and enantioselectively synthesizing nitrogen heterocycles with biological relevance. Copyright

Convergent asymmetric disproportionation reactions: Metal/Bronsted acid relay catalysis for enantioselective reduction of quinoxalines

A convergent asymmetric disproportionation of dihydroquinoxalines for the synthesis of chiral tetrahydroquinoxalines using a metal/Bronsted acid relay catalysis system has been developed. The use of hydrogen gas as the reductant makes the convergent dispr