55408-11-2

Usage

Uses

Used in Organic Synthesis:
5-Chloromethyl-1H-tetrazole is used as a reagent in organic synthesis for its ability to facilitate various chemical reactions, contributing to the formation of complex organic molecules.
Used in Pharmaceutical Industry:
5-Chloromethyl-1H-tetrazole is used as a precursor in the preparation of pharmaceuticals for its role in the synthesis of active pharmaceutical ingredients, enhancing the development of new drugs.
Used in Agricultural Chemicals:
In the agricultural sector, 5-Chloromethyl-1H-tetrazole is used as a precursor to develop compounds that can be utilized in pest control and crop protection, contributing to more effective and targeted agricultural solutions.
Used in Dyes and Coatings Industry:
5-Chloromethyl-1H-tetrazole is used as an intermediate in the production of dyes and coatings, providing a foundation for the creation of colorants and protective layers with specific properties.
Used in Material Science:
5-Chloromethyl-1H-tetrazole is being studied for its potential use in the development of new materials, indicating its versatility beyond traditional applications and suggesting future uses in various industries.
Used as Antimicrobial and Anti-Fungal Agent:
5-Chloromethyl-1H-tetrazole is being explored for its potential as an antimicrobial and antifungal agent, highlighting its possible applications in healthcare and sanitation to combat microbial infections.

InChI:InChI=1/C2H3ClN4/c3-1-2-4-6-7-5-2/h1H2,(H,4,5,6,7)

Upstream product

• 80251-76-9 (1H-tetrazol-5-yl)methanol 
• 107-14-2 chloroacetonitrile 

Downstream Products

• 55408-14-5 5-(chloromethyl)-2-methyl-2H-tetrazole 
• 57235-84-4 1-methyl-5-chloromethyl-1,2,3,4-tetrazole 
• 31602-63-8 (1H-tetrazol-5-yl)methanamine 
• 160998-59-4 (2-triphenylmethyltetrazol-5-yl)methyl chloride 
• 208584-81-0 5-(chloromethyl)-1-(4-methoxybenzyl)-1H-tetrazole 

Relevant academic research and scientific papers

Polynuclear nonfused bis(1,3,4-oxadiazole)-containing systems

Nonfused bis-1,3,4-oxadiazoles were synthesized by reaction of 5-substituted mono- and bis-tetrazoles with mono- and dicarboxylic acid chlorides. The results of kinetic studies showed that the transformation of tetrazoles into 1,3,4-oxadiazoles is accelerated by 1 to 2 orders of magnitude on addition of a catalytic amount of dimethylformamide, triethylamine, or pyridine. Pleiades Publishing, Inc., 2006.

High affinity phenylglycinol-based NK1 receptor antagonists

Heterocyclic replacements for the carboxamido group of the previously disclosed phenylglycinol-based human NK1 (hNK1) receptor antagonists have been investigated, ultimately leading to acyclic compounds with sub-nanomolar affinity for the hNK1 receptor.

4-Me-1-(2-(1H-tetrazol-5-yl)ethyl)benzene sulfonate and N-2-(1H-tetrazol-5-yl)ethyl methanesulfonamide

At least one compound defined by one of the following formulae: STR1 where X represents Cl, Br, STR2 or--SCH3, and n is 1 or 2; and have been administered to animals to improve the efficiency of food utilization by these animals. These compounds can be administered orally by combining the compounds with feed compositions and fed to animals such as ruminants with a developed rumen function as well as other animals that ferment fibrous material and vegetable matter in the cecum or colon. These compounds effect the rumen metabolism to increase the production of propionate relative to other volatile fatty acids, particularly acetate and to inhibit methanogenesis.

Synthese d'analogues tetrazoles de l'acide phosphonoacetique

Several routes to 5-(phosphonomethyl)-1(H)-tetrazole, a new antiviral agent, have been investigated.