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2-Methyl-5-phenyl-3(2H)-isoxazolone is a chemical compound belonging to the isoxazolone family, characterized by a five-membered heterocyclic ring containing an oxygen atom, a nitrogen atom, and a carbonyl group. This specific compound features a methyl group at the 2-position and a phenyl group at the 5-position, which are both substituents attached to the isoxazolone core structure. It is an organic molecule with potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science, due to its unique chemical properties and reactivity. The compound can be synthesized through various methods, including the condensation of α-amino acids with α-keto acids or the reaction of hydroxylamine with α-keto esters. Its chemical formula is C10H9NO2, and it has a molecular weight of 175.184 g/mol.

942-64-3

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942-64-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 942-64-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,4 and 2 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 942-64:
(5*9)+(4*4)+(3*2)+(2*6)+(1*4)=83
83 % 10 = 3
So 942-64-3 is a valid CAS Registry Number.

942-64-3Relevant academic research and scientific papers

Evaluation and Synthesis of Aminohydroxyisoxazoles and Pyrazoles as Potential Glycine Agonists

Drummond, J.,Johnson, G.,Nickell, D. G.,Ortwine, D. F.,Bruns, R. F.,Welbaum, B.

, p. 2116 - 2128 (2007/10/02)

Except for structurally similar small amino acids, such as alanine, β-alanine, and serine, compounds acting as glycine-receptor agonists are an unknown class of pharmacological agents.To investigate the potential of small, substituted heterocycles to act as glycine agonists, we have evaluated the similarities between glycine and a series of hydroxy- and amino-substituted pyrazoles and isoxazoles through complementary molecular modeling techniques.Using a "scorecard approach" to determine the overall similarity of projected agonist structures to glycine, we prioritized synthesis and subsequently prepared several novel derivatives.The biological activity of these compounds was compared to that of glycine by using a strychnine-mediated glycine receptor binding assay.Despite the close similarity in the calculated parameters when compared to glycine, no significant receptor-binding activity was observed for the targeted analogues.These results illustrate the structurally exacting nature of the glycine receptor.

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