Product Name:2-Benzyl-5-(chloromethyl)-1,3,4-oxadiazole

IUPAC Name:2-benzyl-5-(chloromethyl)-1,3,4-oxadiazole

CAS:36646-13-6
Molecular Formula:C10H9ClN2O
Purity:95%+
Catalog Number:CM374188
Molecular Weight:208.65

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CM374188-250mg in stock Ǚƚ
CM374188-1g in stock ǸǸƚ

For R&D use only.

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Product Details

CAS NO:36646-13-6
Molecular Formula:C10H9ClN2O
Melting Point:-
Smiles Code:ClCC1=NN=C(CC2=CC=CC=C2)O1
Density:
Catalog Number:CM374188
Molecular Weight:208.65
Boiling Point:
MDL No:
Storage:

Category Infos

Oxadiazoles
Oxadiazoles are a class of heterocyclic aromatic compounds with the molecular formula C2H2N2O, which have special biological activities and thermodynamic properties. Five-membered heterocyclic moieties composed of three or two heteroatoms are of great interest to researchers because these compounds show significant therapeutic potential. These heterocycles can serve as a building block for the development of novel molecular structures.

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Product Other Information

Product Overview 2-Benzyl-5-(chloromethyl)-1,3,4-oxadiazole (BCMO) is a heterocyclic compound belonging to the oxadiazole class of compounds. It is a five-membered ring system consisting of two nitrogen atoms and one oxygen atom. BCMO is a versatile compound with a wide range of applications in scientific research and laboratory experiments.
Synthesis and Application 2-Benzyl-5-(chloromethyl)-1,3,4-oxadiazole can be synthesized by several different methods. A common approach is the condensation of 2-benzyl-5-chloro-1,3,4-oxadiazole-2-thiol with 2-aminobenzaldehyde, which can be done in the presence of a catalyst such as zinc chloride or piperidine. Another method involves the reaction of 2-chloro-5-methyl-1,3,4-oxadiazole-2-thiol with 2-aminobenzaldehyde in the presence of a catalyst such as zinc chloride or piperidine. The reaction of 2-benzyl-5-chloro-1,3,4-oxadiazole-2-thiol with 2-aminobenzaldehyde in the presence of a catalyst such as zinc chloride or piperidine can also be used to synthesize 2-Benzyl-5-(chloromethyl)-1,3,4-oxadiazole. 2-Benzyl-5-(chloromethyl)-1,3,4-oxadiazole has been used in a variety of scientific research applications. It has been used as a model compound to study the mechanism of action of drugs, as an inhibitor of enzymes, and as a catalyst for chemical reactions. 2-Benzyl-5-(chloromethyl)-1,3,4-oxadiazole has also been used to study the structure and function of proteins and to investigate the interactions between proteins and drugs. Additionally, 2-Benzyl-5-(chloromethyl)-1,3,4-oxadiazole has been used to study the properties of organic compounds and to investigate the synthesis of organic compounds.
Future Directions There are several potential future directions for 2-Benzyl-5-(chloromethyl)-1,3,4-oxadiazole research. One potential direction is the development of new synthesis methods for 2-Benzyl-5-(chloromethyl)-1,3,4-oxadiazole. This could involve the use of new catalysts or the development of new reaction conditions. Additionally, further research could be done on the mechanism of action of 2-Benzyl-5-(chloromethyl)-1,3,4-oxadiazole, as well as its biochemical and physiological effects. Furthermore, research could be done to investigate the use of 2-Benzyl-5-(chloromethyl)-1,3,4-oxadiazole as a drug delivery system or as a therapeutic agent. Finally, research could be done to explore the potential applications of 2-Benzyl-5-(chloromethyl)-1,3,4-oxadiazole in other areas, such as agriculture or food science.