CAS 343566-56-3

3-Isoxazolecarboxylic acid, 5-chloro-, ethyl ester

Description:

3-Isoxazolecarboxylic acid, 5-chloro-, ethyl ester is a chemical compound characterized by its isoxazole ring structure, which is a five-membered heterocyclic compound containing both nitrogen and oxygen. This compound features a carboxylic acid functional group and an ethyl ester moiety, contributing to its reactivity and solubility properties. The presence of a chlorine atom at the 5-position of the isoxazole ring can influence its biological activity and chemical behavior, often enhancing its lipophilicity and potential for interaction with biological targets. Typically, compounds like this may exhibit applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. Its molecular structure allows for various functionalization possibilities, making it a versatile building block in chemical synthesis. Safety and handling precautions should be observed, as with many chemical substances, due to potential toxicity or reactivity. As with any compound, specific characteristics such as melting point, boiling point, and solubility would need to be referenced from reliable chemical databases or literature for detailed applications and safety information.

Formula: C₆H₆ClNO₃

Ethyl 5-chloro-1,2-oxazole-3-carboxylate

CAS: 343566-56-3

Formula: C₆H₆ClNO₃

Purity: 98%

Color and Shape: Liquid

Molecular weight: 175.5697

Ref: IN-DA00VSJ6

Ethyl 5-chloro-1,2-oxazole-3-carboxylate

CAS: 343566-56-3

Ethyl 5-chloro-1,2-oxazole-3-carboxylate

Purity: 98%

Molecular weight: 175.57g/mol

Ref: 54-OR86243

Ethyl 5-chloro-1,2-oxazole-3-carboxylate

CAS: 343566-56-3

Purity: 98%

Molecular weight: 175.5700073

Ref: 10-F648665

Ethyl 5-chloro-1,2-oxazole-3-carboxylate

CAS: 343566-56-3

Ethyl 5-chloro-1,2-oxazole-3-carboxylate is a cytotoxic drug that has been shown to be selective against the virus Coxsackievirus B3. It is a synthetic compound that has been shown to have antiviral activity against Coxsackievirus B3 and pleconaril. The selectivity index of this drug is 0.8. This means that for every 100 compounds with the same biological activity, only 8 are able to inhibit the growth of Coxsackievirus B3. Other modifications include an amide bond between the sulfur atom in ethyl 5-chloro-1,2-oxazole-3-carboxylate and the piperazine group at position 3 on the 1,2 oxazole ring. The linker is a carbon chain with six methyl groups attached to it that can be modified by substituting one or more of these methyl groups with other functional groups such

Formula: C₆H₆ClNO₃

Purity: Min. 95%

Molecular weight: 175.57 g/mol

Ref: 3D-TNA56656