Methyl 2-({[3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolyl]carbonyl}amino)acetate, with the CAS number 349398-65-8, is a chemical compound characterized by its complex structure, which includes an isoxazole ring and a dichlorophenyl group. This compound typically exhibits properties associated with both its functional groups and overall molecular architecture. Isoxazoles are known for their biological activity, often serving as intermediates in pharmaceuticals. The presence of the dichlorophenyl moiety may enhance lipophilicity and influence the compound's interaction with biological targets. Methyl esters, like the acetate in this compound, are generally more soluble in organic solvents and can undergo hydrolysis to yield the corresponding carboxylic acid. The compound's potential applications may include roles in medicinal chemistry, particularly in the development of therapeutic agents. Its stability, reactivity, and specific interactions would depend on the surrounding conditions, such as pH and temperature, as well as the presence of other chemical species.

methyl 2-({[3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolyl]carbonyl}amino)acetate

349398-65-8: Methyl 2-({[3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolyl]carbonyl}amino)acetate, with the CAS number 349398-65-8, is a chemical compound characterized by its complex structure, which includes an isoxazole ring and a dichlorophenyl group. This compound typically exhibits properties associated with both its functional groups and overall molecular architecture. Isoxazoles are known for their biological activity, often serving as intermediates in pharmaceuticals. The presence of the dichlorophenyl moiety may enhance lipophilicity and influence the compound's interaction with biological targets. Methyl esters, like the acetate in this compound, are generally more soluble in organic solvents and can undergo hydrolysis to yield the corresponding carboxylic acid. The compound's potential applications may include roles in medicinal chemistry, particularly in the development of therapeutic agents. Its stability, reactivity, and specific interactions would depend on the surrounding conditions, such as pH and temperature, as well as the presence of other chemical species.

Methyl (3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carbonyl)glycinate

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CAS 349398-65-8

methyl 2-({[3-(2,6-dichlorophenyl)-5-methyl-4-isoxazolyl]carbonyl}amino)acetate

Methyl (3-(2,6-dichlorophenyl)-5-methylisoxazole-4-carbonyl)glycinate

Ref: 10-F727099

methyl 2-((3-(2,6-dichlorophenyl)-5-methylisoxazol-4-yl)carbonylamino)acetate

Ref: 3D-FM169899