36401-55-5

Usage

Uses

Used in Pharmaceutical Industry:
5-METHYL-2-PHENYL-2H-1,2,3-TRIAZOLE-4-CARBONYL CHLORIDE is used as a reagent for the synthesis of various pharmaceuticals. Its unique structure and versatility in chemical reactions allow for the creation of a wide range of biologically active compounds, contributing to the development of new medications.
Used in Agrochemical Industry:
5-METHYL-2-PHENYL-2H-1,2,3-TRIAZOLE-4-CARBONYL CHLORIDE is used as a reagent for the preparation of agrochemicals. Its potential in the synthesis of diverse biologically active compounds makes it a valuable intermediate in the development of new agricultural chemicals.
Used in Medicinal Chemistry and Drug Discovery:
5-METHYL-2-PHENYL-2H-1,2,3-TRIAZOLE-4-CARBONYL CHLORIDE is used as an intermediate for the synthesis of compounds with potential therapeutic applications. Its unique structure and versatility in chemical reactions make it a promising candidate for the development of new drugs and therapeutic agents.
It is important to handle and use 5-METHYL-2-PHENYL-2H-1,2,3-TRIAZOLE-4-CARBONYL CHLORIDE with caution, following proper safety protocols and regulations to ensure the safety of both individuals and the environment.

InChI:InChI=1/C10H8ClN3O/c1-7-9(10(11)15)13-14(12-7)8-5-3-2-4-6-8/h2-6H,1H3

Upstream product

• 22300-56-7 5-methyl-2-phenyl-2H-1,2,3-triazole-4-carboxylic acid 

Downstream Products

• 257875-56-2 N-[3-[2-[bis(1-methylethyl)amino]ethoxy]-4-methoxyphenyl]-5-methyl-2-phenyl-2H-1,2,3-triazole-4-carboxamide 
• 1026766-01-7 C₂₃H₂₃N₇O₂ 
• 1133431-30-7 5-methyl-2-phenyl-2H-[1,2,3]triazole-4-carboxylic acid (3-oxo-1-propyl-2,3-dihydro-1H-indazol-5-yl)-amide 

Relevant academic research and scientific papers

The structural properties of 5-methyl-2-phenyl-2H-1,2,3-triazole-4- carboxylic acid and chromogenic mechanism on its rhodamine B derivatives to Hg2+ ions

5-Methyl-2-phenyl-2H-1,2,3-triazole-4-carboxylic acid (MPTC), a newly synthesized compound, was explored to study the structural properties and theoretical spectra by using GaussView5.0 program package and the time dependent density functional theory (TD

Preparation of novel antibacterial agents. Replacement of the central aromatic ring with heterocycles

Discovery of novel antibacterial agents is a significant challenge. We have recently reported on our discovery of novel antibacterial agents in which we have rapidly optimized potency utilizing a parallel chemistry approach. These advanced leads suffer from high affinity for human serum albumin (HSA). In an effort to decrease the affinity for HSA we have prepared a series of heterocyclic analogs, which retained antibacterial activity and demonstrated reduced affinity for HSA.

HETEROARYL SUBSTITUTED CYCLOHEXYL-1,4-DIAMINE DERIVATIVES

The invention relates to substituted cyclohexyl-1,4-diamine derivatives, a method for the production thereof, medicaments containing these compounds, and to the use of substituted cyclohexyl-1,4-diamine derivatives for producing medicaments.