79960-26-2

Basic information

• Product Name: 2-benzoyl-1-cyano-1,2,3,4-tetrahydro-β-carboline
• Synonyms: 2-benzoyl-1-cyano-1,2,3,4-tetrahydro-β-carboline
• CAS NO: 79960-26-2
• Molecular Weight: 301.348
• Mol File: 79960-26-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2-benzoyl-1-cyano-1,2,3,4-tetrahydro-β-carboline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-benzoyl-1-cyano-1,2,3,4-tetrahydro-β-carboline(79960-26-2)
• EPA Substance Registry System: 2-benzoyl-1-cyano-1,2,3,4-tetrahydro-β-carboline(79960-26-2)

Safety Data

• Hazardous Substances Data: 79960-26-2(Hazardous Substances Data)

Upstream product

• 98-88-4 benzoyl chloride 
• 4894-26-2 3,4-dihydro-β-carboline 
• 79960-38-6 1-amino-3-phenyl-5,6-dihydro-11H-oxazolo<3',4':1,2>pyrido<3,4-b>indol-4-ium chloride 
• 7677-24-9 trimethylsilyl cyanide 

Downstream Products

• 38940-60-2 9H-pyrido[3,4-b]indole-1-carboxamide 
• 79960-41-1 dimethyl 3-phenyl-5,6-dihydro-11H-pyrrolo<1',2':1,2>pyrido<3,4-b>indole-1,2-dicarboxylate 
• 79960-42-2 dimethyl 3-phenyl-11H-pyrrolo<1',2':1,2>pyrido<3,4-b>indole-1,2-dicarboxylate 
• 76945-01-2 2-benzoyl-1-cyano-1,9-dimethyl-1,2,3,4-tetrahydro-β-carboline 
• 79960-31-9 3-benzoyl-3a-cyano-1,2,3,3a,4,9-hexahydro<2>benzazepino<2,3,4-lm>-β-carboline 
• 79960-30-8 3-benzoyl-3a-cyano-2,3,3a,4,5,6-hexahydro-1H-indolo<3,2,1-de><1,5>naphthyridine 
• 79960-29-5 2-Benzoyl-1,9-bis-(4-bromo-benzyl)-2,3,4,9-tetrahydro-1H-β-carboline-1-carbonitrile 
• 79979-35-4 1,9-Diallyl-2-benzoyl-2,3,4,9-tetrahydro-1H-β-carboline-1-carbonitrile 
• 79960-38-6 1-amino-3-phenyl-5,6-dihydro-11H-oxazolo<3',4':1,2>pyrido<3,4-b>indol-4-ium chloride 
• 79960-27-3 2-Benzoyl-1,9-dibenzyl-2,3,4,9-tetrahydro-1H-β-carboline-1-carbonitrile 

Relevant articles and documents

Reissert Compound Studies. XLII. Synthesis and Reactions of the 3,4-Dihydro-β-carboline Reissert Compound and Observations on α, β, and γ-Carbolines

3,4-Dihydro-β-carboline and benzo-γ-carboline yielded Reissert compounds.The 3,4-dihydro-β-carboline Reissert compound, through its acid- and base-promoted reactions, was found to be a very useful intermediate in the synthesis of several β-carboline de