99280-81-6

Basic information

• Product Name: methyl 3,4-dimethoxybenzenecarboximidate hydrochloride
• Synonyms: methyl 3,4-dimethoxybenzenecarboximidate hydrochloride
• CAS NO: 99280-81-6
• Molecular Weight: 231.679
• Mol File: 99280-81-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: methyl 3,4-dimethoxybenzenecarboximidate hydrochloride(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 3,4-dimethoxybenzenecarboximidate hydrochloride(99280-81-6)
• EPA Substance Registry System: methyl 3,4-dimethoxybenzenecarboximidate hydrochloride(99280-81-6)

Safety Data

• Hazardous Substances Data: 99280-81-6(Hazardous Substances Data)

Upstream product

• 67-56-1 methanol 
• 2024-83-1 veratronitrile 

Downstream Products

• 53292-69-6 2-(3,4-dimethoxyphenyl)-1H-imidazole-4-methanol 
• 51488-33-6 3,4-dimethoxy benzenecarboximidamide hydrochloride 
• 882517-80-8 5-(2-amino-5-chlorophenyl)-3-(3,4-dimethoxyphenyl)-1H-1,2,4-triazole 
• 99280-82-7 2-(3,4-Dimethoxy-phenyl)-1H-imidazole-4-carbaldehyde 
• 99280-79-2 [2-(3,4-Dimethoxy-phenyl)-1-methyl-1H-imidazol-4-yl]-methanol 
• 99280-84-9 2-(3,4-Dimethoxy-phenyl)-3-methyl-3H-imidazole-4-carbaldehyde 
• 99280-83-8 2-(3,4-Dimethoxy-phenyl)-1-methyl-1H-imidazole-4-carbaldehyde 
• 99280-92-9 2-(3,4-dimethoxyphenyl)-1-methyl-γ-oxo-1H-imidazole-4-butanenitrile 
• 99280-94-1 2-(3,4-dimethoxyphenyl)-1-methyl-γ-oxo-1H-imidazole-4-butanoic acid 
• 99280-86-1 α-<2-(3,4-dimethoxyphenyl)-1-methyl-1H-imidazol-4-yl>-4-morpholineacetonitrile 
• 99280-90-7 2-<2-(3,4-dimethoxyphenyl)-1-methyl-1H-imidazol-4-yl>-2-(4-morpholinyl)pentanedinitrile 

Relevant articles and documents

Synthesis and evaluation of adenosine antagonist activity of a series of [1,2,4]triazolo[1,5-c]quinazolines

A series of [1,2,4]triazolo[1,5-c]quinazolines were prepared in satisfactory yields by reaction of some derivatives of 2-aminobenzohydrazide with several hydrochlorides of aromatic amidines, and their binding affinities for the recombinant human adenosine A2A and A2B receptors were determined. None of the new compounds showed noteworthy affinity for these receptors, though a very high affinity for the A2A receptor and, consequently, a high level of A2A/A2B selectivity was revealed for one of the synthesized compounds.