5315-72-0

Basic information

• Product Name: methyl 1-phenyl-1H-1,2,3-triazole-5-carboxylate
• Synonyms: methyl 1-phenyl-1H-1,2,3-triazole-5-carboxylate
• CAS NO: 5315-72-0
• Molecular Weight: 203.2
• Mol File: 5315-72-0.mol

Chemical Properties

• CAS DataBase Reference: methyl 1-phenyl-1H-1,2,3-triazole-5-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 1-phenyl-1H-1,2,3-triazole-5-carboxylate(5315-72-0)
• EPA Substance Registry System: methyl 1-phenyl-1H-1,2,3-triazole-5-carboxylate(5315-72-0)

Safety Data

• Hazardous Substances Data: 5315-72-0(Hazardous Substances Data)

Upstream product

• 4967-77-5 methyl 1,2,3-triazole-4-carboxylate 
• 71-43-2 benzene 
• 52745-92-3 methyl (E)-3-nitroacrylate 
• 622-37-7 Phenyl azide 
• 922-67-8 propynoic acid methyl ester 
• 62-53-3 aniline 
• 7377-75-5 methyl 3-phenylamino-2-propenoate 
• 68418-90-6 β-nitroacrylate de methyle 

Downstream Products

• 942-24-5 3-methoxycarbonylindole 
• 1202-04-6 indole-2-carboxylic acid methyl ester 

Relevant articles and documents

Unveiling Potent Photooxidation Behavior of Catalytic Photoreductants

We describe a photocatalytic system that reveals latent photooxidant behavior from one of the most reducing conventional photoredox catalysts, N-phenylphenothiazine (PTH). This aerobic photochemical reaction engages difficult to oxidize feedstocks, such as benzene, in C(sp2)-N coupling reactions through direct oxidation. Mechanistic studies are consistent with activation of PTH via photooxidation and with Lewis acid cocatalysts scavenging inhibitors inextricably formed in this process.

The azide-alkyne cycloaddition catalysed by transition metal oxide nanoparticles

Colloidal nanoparticles of Earth-abundant, first-row transition metal oxides and sulfide, namely magnetite (Fe3O4), manganese and cobalt ferrite, (MnFe2O4, CoFe2O4), manganese(ii) oxide (Mn

TBAI or KI-Promoted Oxidative Coupling of Enamines and N-Tosylhydrazine: An Unconventional Method toward 1,5- and 1,4,5-Substituted 1,2,3-Triazoles

A novel method for the synthesis of 1,5- and 1,4,5-substituted 1,2,3-triazoles has been reported. This approach is promoted by iodine-TBHP oxidation system using enamines and N-tosylhydrazine as materials, which avoid the dependence of traditional methods on azides and transition metals. Through this approach, various 1,5- and 1,4,5-substituted 1,2,3-triazoles were delivered in moderate to high yields. The mechanistic study indicated that an amino exchange would be involved in the reaction process. Moreover, the product methyl 1-(2-methoxyphenyl)-4-methyl-1H-1,2,3-triazole-5-carboxylate is a useful precursor to anti-influenza A agent, and further application research was conducted. (Figure presented.).

Pressure-accelerated azide-alkyne cycloaddition: Micro capillary versus autoclave reactor performance

Pressure effects on regioselectivity and yield of cycloaddition reactions have been shown to exist. Nevertheless, high pressure synthetic applications with subsequent benefits in the production of natural products are limited by the general availability o

3-nitro- and 3-bromo-3-nitroacrylates in reactions with phenyl azide

1,3-Dipolar cycloaddition of alkyl 3-nitro-and 3-bromo-3-nitroacrylates to phenyl azide gives regioisomeric alkyl 5(4)-nitro-1-phenyl-4,5-dihydro-1H-1,2,3- triazole-4(5)-carboxylates, the corresponding triazoles both with and without nitro group, and alky

Arylazide cycloaddition to methyl propiolate: DFT-based quantitative prediction of regioselectivity

Several 1-(4-substituted)-phenyl-4- or 5-methoxycarbonyl-1,2,3-triazoles have been synthesized by 1,3-dipolar cycloaddition of the corresponding arylazides to methyl propiolate in carbon tetrachloride. The regioselectivity of these reactions cannot be rat

CYCLOADDITION DES METHYLAZIDE ET PHENYLAZIDE AU β-NITROSTYRENE ET AU NITROPROPENE HOMOLOGUE

Phenylazide and methylazide reacts with title olefines and gives two isomeric triazoles without nitro group, and 4-nitro-1,2,3 triazole.The isomerisation of starting alkenes explains the formation of isomeric triazoles.Oxydation of amino-nitro-diazocompounds in equilibrium with 1,2,3 triazolines leads to 4-nitro-1,2,3 triazoles.