5-Methyl-2-Phenyl-2H-1,2,3-Triazole-4-Carbonyl Chloride

95%

Reagent Code: #210320
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CAS Number 36401-55-5

science Other reagents with same CAS 36401-55-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.64 g/mol
Formula C₁₀H₈ClN₃O
badge Registry Numbers
MDL Number MFCD00052545
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used primarily as an intermediate in organic synthesis, this compound is valuable in the preparation of pharmaceuticals and agrochemicals. Its reactive carbonyl chloride group readily forms amide, ester, and other derivatives, making it useful in constructing biologically active molecules. It is employed in the development of triazole-based drugs, which often exhibit antimicrobial, antifungal, or anti-inflammatory properties. Additionally, it serves in the synthesis of ligands for catalysis and in the creation of functional materials where the triazole ring acts as a stable heterocyclic scaffold.

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inventory 100mg
10-20 days ฿7,670.00

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5-Methyl-2-Phenyl-2H-1,2,3-Triazole-4-Carbonyl Chloride
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Used primarily as an intermediate in organic synthesis, this compound is valuable in the preparation of pharmaceuticals and agrochemicals. Its reactive carbonyl chloride group readily forms amide, ester, and other derivatives, making it useful in constructing biologically active molecules. It is employed in the development of triazole-based drugs, which often exhibit antimicrobial, antifungal, or anti-inflammatory properties. Additionally, it serves in the synthesis of ligands for catalysis and in the cr

Used primarily as an intermediate in organic synthesis, this compound is valuable in the preparation of pharmaceuticals and agrochemicals. Its reactive carbonyl chloride group readily forms amide, ester, and other derivatives, making it useful in constructing biologically active molecules. It is employed in the development of triazole-based drugs, which often exhibit antimicrobial, antifungal, or anti-inflammatory properties. Additionally, it serves in the synthesis of ligands for catalysis and in the creation of functional materials where the triazole ring acts as a stable heterocyclic scaffold.

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