84218-39-3

Basic information

• Product Name: 2(1H)-Isoquinolinemethanamine, 3,4-dihydro-N-(4-chlorophenyl)-6,7-dime thoxy-1-(1H-indol-3-ylmethyl)-
• Synonyms: 2(1H)-Isoquinolinemethanamine, 3,4-dihydro-N-(4-chlorophenyl)-6,7-dime thoxy-1-(1H-indol-3-ylmethyl)-
• CAS NO: 84218-39-3
• Molecular Formula: C27H28 Cl N3 O2
• Molecular Weight: 0
• Mol File: 84218-39-3.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 670.4°C at 760 mmHg
• Flash Point: 359.2°C
• Appearance: /
• Density: 1.272g/cm³
• Vapor Pressure: 7.78E-18mmHg at 25°C
• Refractive Index: 1.669
• CAS DataBase Reference: 2(1H)-Isoquinolinemethanamine, 3,4-dihydro-N-(4-chlorophenyl)-6,7-dime thoxy-1-(1H-indol-3-ylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Isoquinolinemethanamine, 3,4-dihydro-N-(4-chlorophenyl)-6,7-dime thoxy-1-(1H-indol-3-ylmethyl)-(84218-39-3)
• EPA Substance Registry System: 2(1H)-Isoquinolinemethanamine, 3,4-dihydro-N-(4-chlorophenyl)-6,7-dime thoxy-1-(1H-indol-3-ylmethyl)-(84218-39-3)

Safety Data

• Hazardous Substances Data: 84218-39-3(Hazardous Substances Data)

Usage

Core Structure

Isoquinoline

Molecular Structure

The compound contains a 3,4-dihydroisoquinoline core structure with a 4-chlorophenyl and 1H-indol-3-ylmethyl substituent at different positions of the molecule.

Pharmacological Effects

The compound has been studied for its potential therapeutic properties, including its antiproliferative and anti-inflammatory effects.

Potential Applications

The compound may have potential applications in the treatment of various diseases, including cancer and neurodegenerative disorders.

Further Research

Further research is needed to fully understand the pharmacological effects and therapeutic potential of this compound.

InChI:InChI=1/C27H28ClN3O2/c1-32-26-14-18-11-12-31(17-30-21-9-7-20(28)8-10-21)25(23(18)15-27(26)33-2)13-19-16-29-24-6-4-3-5-22(19)24/h3-10,14-16,25,29-30H,11-13,17H2,1-2H3

Upstream product

• 13433-48-2 N-(2-(3,4-dimethoxyphenyl)ethyl)-2-(1H-indol-3-yl)acetamide 
• 120-20-7 2-(3,4-dimethoxyphenyl)-ethylamine 
• 87-51-4 indole-3-acetic acid 
• 50-00-0 formaldehyd 
• 106-47-8 4-chloro-aniline 
• 15832-21-0 1-((1H-indol-3-yl)methyl)-6,7-dimethoxy-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

Antiinflammatory and antiproteolytic activities of newer indolyl isoquinolines

Several indolyl isoquinoline derivatives were synthesized and evaluated for their antiinflammatory and antiproteolytic activities. These derivatives possessed 9.2-32.4% inhibition at a dose of 100 mg/kg i.p. against carrageenin-induced oedema. Four of the