100252-79-7

Basic information

• Product Name: 3-(3,4,5-trimethoxyphenyl)propan-1-amine
• Synonyms: 3-(3,4,5-trimethoxyphenyl)propan-1-amine
• CAS NO: 100252-79-7
• Molecular Weight: 225.288
• Mol File: 100252-79-7.mol

Chemical Properties

• CAS DataBase Reference: 3-(3,4,5-trimethoxyphenyl)propan-1-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3,4,5-trimethoxyphenyl)propan-1-amine(100252-79-7)
• EPA Substance Registry System: 3-(3,4,5-trimethoxyphenyl)propan-1-amine(100252-79-7)

Safety Data

• Hazardous Substances Data: 100252-79-7(Hazardous Substances Data)

Upstream product

• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 49621-49-0 3,4,5-trimethoxycinnamyl nitrile 
• 49621-50-3 3-(3,4,5-Trimethoxyphenyl)propionitrile 
• 90-50-6 3,4,5-trimethoxycinnamic acid 
• 53560-26-2 3-(3,4,5-trimethoxyphenyl)propan-1-ol 
• 117824-56-3 wikstromol 
• 117824-62-1 N-[3-(3,4,5-Trimethoxy-phenyl)-propyl]-benzenesulfonamide 
• 106213-58-5 3-(3,4,5-trimethoxyphenyl)propanamide 

Relevant articles and documents

8-Hydroxyquinolin-2(1H)-one analogues as potential β2-agonists: Design, synthesis and activity study

β2-Agonists that bind to plasmalemmal β2-adrenoceptors causing cAMP accumulation are widely used as bronchodilators in chronic respiratory diseases. Here, we designed and synthesized a group of 8-hydroxyquinolin-2(1H)-one analogues and studied their β2-agonistic activities with a cellular cAMP assay. Compounds B05 and C08 were identified as potent (EC50 2-agonists among the compounds tested. They behaved as partial β2-agonists in non-overexpressed HEK293 cells, and possessed rapid smooth muscle relaxant actions and long duration of action in isolated guinea pig tracheal strip preparations. In summary, B05 and C08 are β2-agonists with potential applicability in chronic respiratory diseases.

NOVEL ALLOSTERIC INHIBITORS OF PROTEASOME AND METHODS OF USE THEREOF

The present invention relates generally to novel allosteric regulators of proteasome activity, methods for preparation and use, and pharmaceutical compositions thereof. Specifically piperidine-2-carboxylic acid derivatives containing 1-oxo-aroyl group and

A USEFUL APPROACH TO PRIMARY AMINES

Smooth reduction of acylsulfonamides to sulfonamides by borane, when coupled to standard sulfonamide cleavage procedures, provides a general route to primary amines.