4953-05-3

Basic information

• Product Name: dimethyl 1-(4-methoxyphenyl)-1H-1,2,3-triazole-4,5-dicarboxylate
• Synonyms: dimethyl 1-(4-methoxyphenyl)-1H-1,2,3-triazole-4,5-dicarboxylate
• CAS NO: 4953-05-3
• Molecular Weight: 291.263
• Mol File: 4953-05-3.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: dimethyl 1-(4-methoxyphenyl)-1H-1,2,3-triazole-4,5-dicarboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl 1-(4-methoxyphenyl)-1H-1,2,3-triazole-4,5-dicarboxylate(4953-05-3)
• EPA Substance Registry System: dimethyl 1-(4-methoxyphenyl)-1H-1,2,3-triazole-4,5-dicarboxylate(4953-05-3)

Safety Data

• Hazardous Substances Data: 4953-05-3(Hazardous Substances Data)

Upstream product

• 947-57-9 dimethyl bicyclo[2.2.1]hept-2,5-diene-2,3-dicarboxylate 
• 2101-87-3 p-methoxy-phenylazide 
• 104-94-9 4-methoxy-aniline 
• 762-42-5 dimethyl acetylenedicarboxylate 
• 1829-60-3 dimethyl 7-oxabicyclo[2.2.1]hepta-2,5-diene-2,3-dicarboxylate 
• 19019-88-6 7-isopropylidene-2,3-dicarbomethoxynorbornadiene 

Downstream Products

• 129748-87-4 Isopropyl-carbamic acid 5-isopropylcarbamoyloxymethyl-3-(4-methoxy-phenyl)-3H-[1,2,3]triazol-4-ylmethyl ester 
• 129748-82-9 [5-Hydroxymethyl-3-(4-methoxy-phenyl)-3H-[1,2,3]triazol-4-yl]-methanol 

Relevant articles and documents

Synthesis and chemiluminescent activity of pyridazino[4,5-b]indole-1,4(2H,3H)-diones

Substituted and non-substituted anilines were transformed to the corresponding triazole derivatives, which were converted to dimethyl indole-2,3-dicarboxylates by photocyclization. The reaction of diester with hydrazine hydrate gave 1,2,3,4-tetrahydro-5H-

SITE SELECTIVITY IN THE REACTIONS OF 1,3-DIPOLES WITH NORBORNADIENE DERIVATIVES

The cycloadditions of arylazides, benzonitrile oxides and diphenylnitrile imine to norbornadiene derivatives 1a-c showed varying degree of site- and stereo-selectivity.With dipolarophile 1a arylazides and benzonitrile oxides attack, preferentially, the electron-poor tetrasubstituted double bond, while in the case of 1b and 1c is the substituted double bond which enters the cycloaddition.By contrast, 2-diazopropane and C-phenyl-N-methylnitrone react with the sole tetrasubstituted double bond of 1a-c in stereo- and site-specific cycloadditions.The quantitative evaluation of the two possible reaction paths was performed by glc analysis.The compounds detected were those arising from Diels-Alder cycloreversions of the thermally labile intermediate adducts 2 and 3 (Scheme 1).The results were rationalized on the basis of a qualitative perturbation treatment which considers frontier orbital interactions only.