55408-11-2 Usage
Description
5-Chloromethyl-1H-tetrazole is a chemical compound characterized by the molecular formula C2H3ClN4. It is a white solid that exhibits solubility in water. 5-Chloromethyl-1H-tetrazole serves as a versatile reagent in organic synthesis and is recognized for its potential as a precursor in the synthesis of pharmaceuticals, agricultural chemicals, dyes, and coatings. Its applications are diverse, extending to the development of new materials and its exploration as an antimicrobial and antifungal agent. However, due to its potential hazards, careful handling is essential.
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.
Check Digit Verification of cas no
The CAS Registry Mumber 55408-11-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,4,0 and 8 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 55408-11:
(7*5)+(6*5)+(5*4)+(4*0)+(3*8)+(2*1)+(1*1)=112
112 % 10 = 2
So 55408-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C2H3ClN4/c3-1-2-4-6-7-5-2/h1H2,(H,4,5,6,7)
55408-11-2Relevant articles and documents
Polynuclear nonfused bis(1,3,4-oxadiazole)-containing systems
Vereshchagin,Petrov,Kizhnyaev,Pokatilov,Smirnov
, p. 1049 - 1055 (2007/10/03)
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.
4-Me-1-(2-(1H-tetrazol-5-yl)ethyl)benzene sulfonate and N-2-(1H-tetrazol-5-yl)ethyl methanesulfonamide
-
, (2008/06/13)
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.