82342-56-1

Basic information

• Product Name: Isoquinoline, 2-benzoyl-1,2,3,4-tetrahydro-
• CAS NO: 82342-56-1
• Molecular Formula: C16H15NO
• Molecular Weight: 237.301
• Mol File: 82342-56-1.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: Isoquinoline, 2-benzoyl-1,2,3,4-tetrahydro-(CAS DataBase Reference)
• NIST Chemistry Reference: Isoquinoline, 2-benzoyl-1,2,3,4-tetrahydro-(82342-56-1)
• EPA Substance Registry System: Isoquinoline, 2-benzoyl-1,2,3,4-tetrahydro-(82342-56-1)

Safety Data

• Hazardous Substances Data: 82342-56-1(Hazardous Substances Data)

Upstream product

• 2744-08-3 decahydroisoquinoline 
• 98-88-4 benzoyl chloride 
• 50-00-0 formaldehyd 
• 3278-14-6 N-phenethylbenzamide 
• 5653-11-2 α-(1,2,3,4-Tetrahydro-2-isochinolyl)-acetophenon 
• 611-73-4 Benzoylformic acid 
• 91-21-4 1,2,3,4-tetrahydroisoquinoline 
• 63412-06-6 N-methyl-N-nitrosobenzamide 
• 88070-48-8 N-methylbenzamide 
• 55-21-0 benzamide 
• 100-52-7 benzaldehyde 
• 65-85-0 benzoic acid 
• 93-89-0 benzoic acid ethyl ester 
• 591-50-4 iodobenzene 

Downstream Products

• 62172-57-0 2-benzoyl-1,2,3,4-tetrahydroisoquinoline-1-carbonitrile 
• 1428485-07-7 C₂₄H₂₁NO₂ 
• 1260507-07-0 phenyl-(1-(2,4,6-trimethoxyphenyl)-3,4-dihydroisoquinolin-2(1H)-yl)methanone 
• 91-21-4 1,2,3,4-tetrahydroisoquinoline 
• 827320-73-0 (1-(1H-Indol-3-yl)-3,4-dihydroisoquinolin-2(1H)-yl)(phenyl)-methanone 
• 88630-43-7 N-propyl-N'-tetrahydroisoquinolinylurea 

Relevant articles and documents

Generation of Oxyphosphonium Ions by Photoredox/Cobaloxime Catalysis for Scalable Amide and Peptide Synthesis in Batch and Continuous-Flow

Phosphine-mediated deoxygenative nucleophilic substitutions, such as the Mitsunobu reaction, are of great importance in organic synthesis. However, the conventional protocols require stoichiometric oxidants to trigger the formation of the oxyphosphonium i

Visible-Light-Mediated Oxidative Amidation of Aldehydes by Using Magnetic CdS Quantum Dots as a Photocatalyst

A magnetic CdS quantum dot (Fe3O4/polydopamine (PDA)/CdS) was synthesized through a facile and convenient method from inexpensive starting materials. Characterization of the prepared catalyst was performed by means of FTIR spectrosco

Tert -Butyl nitrite promoted transamidation of secondary amides under metal and catalyst free conditions

A mild and efficient method is demonstrated for the transamidation of secondary amides with various amines including primary, secondary, cyclic and acyclic amines in the presence of tert-butyl nitrite. The reaction proceeds through the N-nitrosamide intermediate and provides the transamidation products in good to excellent yields at room temperature. Moreover, the developed methodology does not require any catalyst or additives.