15922-67-5

Upstream product

• 1516-60-5 4-nitrophenyl azide 
• 105-45-3 acetoacetic acid methyl ester 

Downstream Products

• 117714-36-0 5-Formyl-4-methoxycarbonyl-1-(p-nitrophenyl)-1,2,3-triazole 
• 117694-03-8 5-Diazomethyl-4-methoxycarbonyl-1-(p-nitrophenyl)-1,2,3-triazole 
• 117693-95-5 5-Azidomethyl-4-methoxycarbonyl-1-(p-nitrophenyl)-1,2,3-triazole 
• 117694-07-2 7-Methoxycarbonyl-7-(1-p-nitrophenyl-1,2,3-triazole-5-yl)-norcardiene 
• 117694-00-5 4-Methoxycasrbonyl-1-(p-nitrophenyl)-1,2,3-triazole-5-carbaldehyde p-tosylhydrazone 
• 1422423-73-1 4-(decyloxy)phenyl 5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazole-4-carboxylate 
• 88958-24-1 C₁₀H₇ClN₄O₃ 
• 1217-99-8 5-methyl-1-(4-nitrophenyl)-1H-1,2,3-triazole-4-carboxylic acid 
• 1392400-58-6 dimethyl 5,5'-((1E,3Z)-4-(dimethylamino)buta-1,3-diene-1,3-diyl)bis(1-(4-nitrophenyl))-1H-1,2,3-triazole-4-carboxylate 
• 1392400-53-1 (E)-methyl 5-(2-(dimethylamino)vinyl)-1-(4-nitrophenyl)-1H-1,2,3-triazole-4-carboxylate 
• 117693-92-2 5-Bromomethyl-4-methoxycarbonyl-1-(p-nitrophenyl)-1,2,3-triazole 
• 117693-93-3 5-Dibromo-4-methoxycarbonyl-1-(p-nitrophenyl)-1,2,3-triazole 

Relevant academic research and scientific papers

Catalytic behavior of surfactant-containing-MCM-41 mesoporousmaterials for cycloaddition of 4-nitrophenyl azide

Si-MCM-41, Ga-MCM-41 and Al-MCM-41 mesoporous catalysts (with Si/Al = 80 and Si/Ga = 80) were pre-pared by direct synthesis under hydrothermal crystallization method using sodium aluminate or galliumsulfate and tetraethyl orthosilicate (TEOS) as aluminum

Efficient, green and regioselective synthesis of 1,4,5-trisubstituted-1,2, 3-triazoles in ionic liquid [bmim]BF4 and in task-specific basic ionic liquid [bmim]OH

Convenient and environmentally benign procedures have been reported for the synthesis of 1,4,5-trisubstituted-1,2,3-triazoles by the reaction of aryl azides with active methylene compounds in ionic liquid [bmim]BF4 in the presence of l-proline

Synthesis of biologically as well as industrially important 1,4,5-trisubstituted-1,2,3-triazoles using a highly efficient, green and recyclable DBU-H2O catalytic system

Substituted 1,2,3-triazoles are important heterocyclic molecules with applications in diverse research areas. 1,3-Dipolar cycloaddition reaction of azides and enolizable compounds is an important method of generating substituted 1,2,3-triazoles. However,

Efficient TMG catalyzed synthesis of 1,2,3-triazoles

A practical and efficient method for the synthesis of 1,2,3-triazoles via the cycloaddition reaction of azides and CH-acids in the presence of 1,1,3,3-tetramethylguanidine (TMG) in ethanol at 30 C has been reported. The simple experimental procedure, shor

Synthesis and mesomorphic properties of novel [1,2,3]-triazole mesogenic based compounds

A series of five-membered heterocyclic 1,2,3-triazole derivatives with different substituents in N1 position was synthesized. The heterocyclic moiety was connected through an ester function to a p-decyloxyphenyl or p-decyloxybiphenyl tails Polarized micro

A combined experimental and theoretical study of the thermal cycloaddition of aryl azides with activated alkenes

Reactions were performed from aryl azides on the one hand, and activated alkenes coming from β-dicarbonyl compounds or malonodinitrile on the other hand, either with recourse to conventional heating or to microwave activation, to afford 1-aryl-1H-1,2,3-tr

DIAZO GROUP TRANSFER AND/OR TRIAZOLE FORMATION IN THE REACTION OF TOLUENE-4-SULPHONYL OR 4-NITROPHENYL AZIDE WITH α-METHYLENE β-DICARBONYL COMPOUNDS IN HEXAMETHYLPHOSPHORIC TRIAMIDE

In hexamethylphosphoric triamide, toluene-4-sulphonyl azide generally performs smooth diazo group transfer to β-dicarbonyl compounds, whereas 4-nitrophenyl azide can exhibit diazo transfer reaction with malonates and cyclic β-diones but leads to triazole formation with acyclic β-diones and β-keto esters.

SYNTHESIS AND THERMAL REARRANGEMENT OF 5-DIAZOMETHYL-1,2,3-TRIAZOLES

5-Diazomethyl-4-methoxycarbonyltriazoles are capable of undergoing ring-degenerate rearrangements (19+20) when a strong electron withdrawing substituent (e.g. p-nitrophenyl or o,p-dinitrophenyl) is located at the N-1 position.Whereas the unrearranged diaz