61001-31-8

Basic information

• Product Name: 2-Phenyl-5,6-dihydropyrazolo[5,1-a]isoquinoline
• Synonyms: 2-Phenyl-5,6-dihydropyrazolo[5,1-a]isoquinoline;5,6-Dihydro-2-phenylpyrazolo[5,1-a]isoquinoline
• CAS NO: 61001-31-8
• Molecular Formula: C₁₇H₁₄N₂
• Molecular Weight: 246.33
• Mol File: 61001-31-8.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 379.31°C (rough estimate)
• Flash Point: 232.8°C
• Appearance: /
• Density: 1.1223 (rough estimate)
• Vapor Pressure: 2.96E-08mmHg at 25°C
• Refractive Index: 1.5794 (estimate)
• CAS DataBase Reference: 2-Phenyl-5,6-dihydropyrazolo[5,1-a]isoquinoline(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Phenyl-5,6-dihydropyrazolo[5,1-a]isoquinoline(61001-31-8)
• EPA Substance Registry System: 2-Phenyl-5,6-dihydropyrazolo[5,1-a]isoquinoline(61001-31-8)

Safety Data

• Hazardous Substances Data: 61001-31-8(Hazardous Substances Data)

Usage

InChI:InChI=1/C17H14N2/c1-2-7-14(8-3-1)16-12-17-15-9-5-4-6-13(15)10-11-19(17)18-16/h1-9,12H,10-11H2

Upstream product

• 61001-28-3 2-phenyl-5,6-dihydro-pyrazolo<5,1-a>isoquinoline-1-carboxylic acid 
• 39113-01-4 2-amino-3,4-dihydro-1(2H)-isoquinolinone 
• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 83391-31-5 ethyl β<(1-oxo-3,4-dihydro-2H-isoquinolyl)amino>cynnamate 
• 1006061-08-0 (2-phenyl-6,10b-dihydro-5H-pyrazolo[5,1-a]isoquinolin-3-yl)-p-tolylmethanone 
• 1006061-05-7 (3,7b-dihydro-2H-1,1a-diazacyclopropa[a]naphthalen-1-yl)-p-tolylmethanone 
• 536-74-3 phenylacetylene 
• 1006061-06-8 (3,7b-dihydro-2H-1,1a-diazacyclopropa[a]naphthalen-1-yl)-(4-methoxyphenyl)methanone 
• 1006061-07-9 (3,7b-dihydro-2H-1,1a-diazacyclopropa[a]naphthalen-1-yl)-(4-nitrophenyl)methanone 
• 1402665-60-4 2-phenyl-1-(trifluoromethylsulfonyl)-5,6-dihydropyrazolo[5,1-a]isoquinoline 
• 91-21-4 1,2,3,4-tetrahydroisoquinoline 
• 19433-17-1 acetophenone O-acetyloxime 

Downstream Products

• 61001-36-3 2-phenyl-pyrazolo<5,1-a>isoquinoline 

Relevant articles and documents

Regioselectivity Control in the Oxidative Formal [3 + 2] Annulations of Ketoxime Acetates and Tetrohydroisoquinolines

A novel copper-catalyzed oxidative formal [3 + 2] annulations of ketoxime acetates and tetrohydroisoquinolines for the synthesis of fused pyrazoles and imidazoles has been developed. A broad range of important isoquinoline-fused pyrazole and imidazole pro

Regioselective synthesis of pyrazole triflones based on triflyl alkyne cycloadditions

The regioselective synthesis of pyrazole triflones has been achieved by 1,3-dipolar cycloaddition of triflyl alkynes and hydrazonoyl chloride in the presence of Huenig's base. Pyrazolo[5,1-a]isoquinoline triflones were also regioselectively synthesized for the first time via tandem 1,3-dipolar cycloaddition/oxidative aromatization between triflyl alkynes and C,N-cyclic azomethine imines.

Synthesis and pregnancy terminating activity of 2-aryl pyrazolo [5,1-a]isoindoles and isoquinolines

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