72299-68-4

Basic information

• Product Name: 1,2,3,4-TETRAHYDRO-ISOQUINOLIN-7-YLAMINE
• Synonyms: 1,2,3,4-TETRAHYDROISOQUINOLIN-7-AMINE;1,2,3,4-TETRAHYDRO-ISOQUINOLIN-7-YLAMINE;7-Amino-1,2,3,4-tetrahydroisoquinoline;A90100;1,2,3,4-Tetrahydro-7-isoquinolinaMine
• CAS NO: 72299-68-4
• Molecular Formula: C₉H₁₂N₂
• Molecular Weight: 148.2
• Product Categories: pharmacetical
• Mol File: 72299-68-4.mol

Chemical Properties

• Boiling Point: 315.903 °C at 760 mmHg
• Flash Point: 169.23 °C
• Appearance: /
• Density: 1.101 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.6
• Storage Temp.: under inert gas (nitrogen or Argon) at 2–8 °C
• CAS DataBase Reference: 1,2,3,4-TETRAHYDRO-ISOQUINOLIN-7-YLAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,3,4-TETRAHYDRO-ISOQUINOLIN-7-YLAMINE(72299-68-4)
• EPA Substance Registry System: 1,2,3,4-TETRAHYDRO-ISOQUINOLIN-7-YLAMINE(72299-68-4)

Safety Data

• Hazardous Substances Data: 72299-68-4(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
1,2,3,4-Tetrahydro-isoquinolin-7-ylamine is used as a pharmaceutical compound for its potential interaction with neurotransmitter receptors in the brain. This interaction may contribute to the development of new treatments for neurological disorders and conditions.
Used in Chemical Synthesis:
1,2,3,4-Tetrahydro-isoquinolin-7-ylamine is used as a precursor in the synthesis of other organic compounds. Its unique structure and functional groups make it a valuable building block for creating new molecules with specific properties and applications.

InChI:InChI=1/C9H12N2/c10-9-2-1-7-3-4-11-6-8(7)5-9/h1-2,5,11H,3-4,6,10H2

Upstream product

• 42923-79-5 7-nitro-1,2,3,4-tetrahydroisoquinoline 
• 186390-77-2 6-nitro-1,2,3,4-tetrahydro-isoquinoline 

Downstream Products

• 149355-52-2 7-cyano-1,2,3,4-tetrahydroisoquinoline 
• 1072084-79-7 7-(4-chloro-6-morpholin-4-yl-pyrimidin-2-ylamino)-3,4-dihydro-1H-isoquinoline-2-carboxylic acid benzyl ester 
• 30798-64-2 7-hydroxy-1,2,3,4-tetrahydroisoquinoline 
• 1139884-67-5 7-(benzyloxycarbonylamino)-1,2,3,4-tetrahydroisoquinoline 
• 81885-67-8 2-acetyl-7-amino-1,2,3,4-tetrahydro-isoquinoline 
• 787640-41-9 benzyl 7-amino-3,4-dihydroisoquinoline-2(1H)-carboxylate 
• 200137-84-4 N-(2-Trityl-1,2,3,4-tetrahydro-isoquinolin-7-ylmethyl)-methanesulfonamide 
• 200137-83-3 C-(2-Trityl-1,2,3,4-tetrahydro-isoquinolin-7-yl)-methylamine 
• 200137-82-2 2-Trityl-1,2,3,4-tetrahydro-isoquinoline-7-carbonitrile 
• 220247-64-3 7-methylsulfonyl-N-triphenylmethyl-1,2,3,4-tetrahydroisoquinoline 
• 220247-62-1 7-bromo-N-triphenylmethyl-1,2,3,4-tetrahydroisoquinoline 
• 220247-55-2 7-methanesulfonyl-1,2,3,4-tetrahydro-isoquinoline 
• 17680-55-6 7-bromo-1,2,3,4-tetrahydroisoquinoline 

Relevant articles and documents

METHODS FOR IDENTIFICATION OF JAK KINASE INTERACTING MOLECULES AND FOR THE PURIFICATION OF JAK KINASES

The present invention relates to immobilization compounds and methods useful for the identification of JAK interacting compounds or for the purification or identification of JAK.