123685-57-4

Basic information

• Product Name: Prop-2-ynyl-(3,4,5-trimethoxy-phenyl)-amine
• Synonyms: Prop-2-ynyl-(3,4,5-trimethoxy-phenyl)-amine
• CAS NO: 123685-57-4
• Molecular Weight: 221.256
• Mol File: 123685-57-4.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Prop-2-ynyl-(3,4,5-trimethoxy-phenyl)-amine(CAS DataBase Reference)
• NIST Chemistry Reference: Prop-2-ynyl-(3,4,5-trimethoxy-phenyl)-amine(123685-57-4)
• EPA Substance Registry System: Prop-2-ynyl-(3,4,5-trimethoxy-phenyl)-amine(123685-57-4)

Safety Data

• Hazardous Substances Data: 123685-57-4(Hazardous Substances Data)

Upstream product

• 106-96-7 propargyl bromide 
• 24313-88-0 3,4,5-Trimethoxyaniline 

Downstream Products

• 123685-28-9 6-[[2-Propynyl-(3,4,5-trimethoxyphenyl)amino]methyl]-4(3H)-quinazolinone 
• 206561-41-3 2,2-Dimethyl-N-(3-phenyl-7-{[prop-2-ynyl-(3,4,5-trimethoxy-phenyl)-amino]-methyl}-quinoxalin-2-yl)-propionamide 
• 123685-32-5 2-amino-6-[[2-propynyl(3,4,5-trimethoxyphenyl)amino]methyl]-4(3H)-quinazolinone 
• 123685-42-7 <4-oxo-6-<<2-propynyl(3,4,5-trimethoxyphenyl)amino>methyl>-3(4H)-quinazolinyl>methyl 2,2-dimethylpropanoate 

Relevant articles and documents

6-Substituted 2,4-diamino-5-methylpyrido[2,3-d]pyrimidines as inhibitors of dihydrofolate reductases from Pneumocystis carinii and Toxoplasma gondii and as antitumor agents

The synthesis and biological activity of 15 6-substituted 2,4-diamino-5- methylpyrido[2,3-d]-pyrimidines are reported. These compounds were synthesized in improved yields by modifications of procedures previously reported by us. Specifically, dimethoxyphe

Synthesis and evaluation of novel fluorinated pyrazolo-1,2,3-triazole hybrids as antimycobacterial agents

A library of novel 3-trifluoromethyl pyrazolo-1,2,3-triazole hybrids (5-7) were accomplished starting from 5-phenyl-3-(trifluoromethyl)-1H-pyrazol-4-amine (1) via key intermediate 2-azido-N-(5-phenyl-3-(trifluoromethyl)-1H-pyrazol-4-yl)acetamide (3) throu

Potent inhibition of thymidylate synthase by two series of nonclassical quinazolines

The synthesis and biological activity of two series of nonclassical thymidylate synthase (TS) inhibitors are described. The first is a series of 10-propargyl-5.8-dideazafolic acid derivatives (10a-j) and the second is a series of the analogous 2-desamino