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3-Methoxy-5-phenylisoxazole is a heterocyclic organic compound characterized by the presence of an isoxazole ring, which is a five-membered ring containing one oxygen atom and one nitrogen atom. This specific compound features a methoxy group (-OCH3) at the 3-position and a phenyl group (C6H5) at the 5-position of the isoxazole ring. It is a colorless solid with a molecular formula of C10H9NO2 and a molecular weight of 175.184 g/mol. 3-Methoxy-5-phenylisoxazole is synthesized through various methods, such as the condensation of phenylglyoxal with hydroxylamine, and is used as a building block in the synthesis of more complex molecules, particularly in pharmaceuticals and agrochemicals. Its chemical properties include reactivity towards electrophilic aromatic substitution and nucleophilic addition reactions, making it a versatile intermediate in organic synthesis.

942-68-7

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942-68-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 942-68-7 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 8 respectively.
Calculate Digit Verification of CAS Registry Number 942-68:
(5*9)+(4*4)+(3*2)+(2*6)+(1*8)=87
87 % 10 = 7
So 942-68-7 is a valid CAS Registry Number.

942-68-7Relevant 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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