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
• Article Data: 1

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

General Description

1,2,3,4-Tetrahydro-isoquinolin-7-ylamine is a chemical compound with the molecular formula C10H14N2. It is a derivative of isoquinoline and contains an amine group. 1,2,3,4-TETRAHYDRO-ISOQUINOLIN-7-YLAMINE has potential pharmaceutical applications, particularly in the field of neuroscience, due to its ability to interact with neurotransmitter receptors in the brain. It may also have potential as a precursor in the synthesis of other organic compounds. The exact properties and potential uses of 1,2,3,4-tetrahydro-isoquinolin-7-ylamine are still being studied, but it shows promise as a versatile chemical with a range of potential 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

• 17680-55-6 7-bromo-1,2,3,4-tetrahydroisoquinoline 
• 30798-64-2 7-hydroxy-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 
• 149355-52-2 7-cyano-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 

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.