82763-23-3

Basic information

• Product Name: (6-METHOXY-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YL)-PROPYL-AMINE HYDROCHLORIDE
• Synonyms: (6-METHOXY-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YL)-PROPYL-AMINE HYDROCHLORIDE;2-NAPHTHALENAMINE, 1,2,3,4-TETRAHYDRO-6-METHOXY-N-PROPYL-, HYDROCHLORIDE;6-METHOXY-N-PROPYL-2-AMINOTETRALINE HYDROCHLORIDE
• CAS NO: 82763-23-3
• Molecular Formula: C₁₄H₂₁NO
• Molecular Weight: 0
• Mol File: 82763-23-3.mol
• Article Data: 2

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (6-METHOXY-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YL)-PROPYL-AMINE HYDROCHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: (6-METHOXY-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YL)-PROPYL-AMINE HYDROCHLORIDE(82763-23-3)
• EPA Substance Registry System: (6-METHOXY-1,2,3,4-TETRAHYDRO-NAPHTHALEN-2-YL)-PROPYL-AMINE HYDROCHLORIDE(82763-23-3)

Safety Data

• Hazardous Substances Data: 82763-23-3(Hazardous Substances Data)

Upstream product

• 107-10-8 propylamine 
• 2472-22-2 6-methoxy-2-tetralone 

Downstream Products

• 82763-53-9 N-Propyl-N-[4-(3,4-dimethoxybenzoyloxy)butyl]-6-methoxy-1,2,3,4-tetrahydro-2-naphthylamine 

Relevant articles and documents

Spasmolytic Agents. 2. 1,2,3,4-Tetrahydro-2-naphthylamine Derivatives

N--1,2,3,4-tetrahydro-2-naphthylamine derivatives were synthesized from 1,2,3,4-tetrahydro-2-naphthylamines evaluated for their spasmolytic activity.Some of these compounds showed a nerve-selective effect on colon rather than stomach in anesthetized dogs and were found to be equal to or more active than the reference drug (mebeverine).The biological data have indicated some structure-activity relationships.Among these compounds, N-ethyl-N-hexyl>-1,2,3,4-tetrahydro-6-methoxy-2-naphthylamine hydrochloride (63) was found to be the most active spasmolytic agent.