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3-Phenyl-5-piperidinomethylisoxazole is a complex organic compound with the molecular formula C16H20N2O. It is a derivative of isoxazole, a heterocyclic aromatic organic compound containing a five-membered ring with one oxygen and three carbon atoms, and a nitrogen atom. The structure of 3-phenyl-5-piperidinomethylisoxazole features a phenyl group (C6H5) at the 3-position, a piperidinomethyl group (C6H11N) at the 5-position, and an isoxazole ring. 3-phenyl-5-piperidinomethylisoxazole is of interest in the field of medicinal chemistry due to its potential applications as a building block for the synthesis of various pharmaceuticals and agrochemicals. Its unique structure allows for the exploration of its properties and potential interactions with biological targets, making it a valuable compound for further research and development.

1026-60-4

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1026-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1026-60-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,2 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1026-60:
(6*1)+(5*0)+(4*2)+(3*6)+(2*6)+(1*0)=44
44 % 10 = 4
So 1026-60-4 is a valid CAS Registry Number.

1026-60-4Downstream Products

1026-60-4Relevant academic research and scientific papers

Synthesis of 5-bromomethylisoxazoles and their reactions with secondary amines

Aliev

, p. 1192 - 1195 (2007/10/03)

Treating R-3-chloro-4-bromo-2-buten-1-ones with hydroxylamine hydrochloride afforded 3-alkyl(aryl, furyl)-5-bromomethylisoxazoles. By reaction of the latter with secondary amines new previously unknown aminoisoxazoles were synthesized. 2005 Pleiades Publi

Regioisomeric 5(3)-aminomethyl-3(5)-phenylisoxazoles: Synthesis, spectroscopic discrimination, and muscarinic activity

Dannhardt,Lambrecht,Laufer,Mutschler,Schweiger

, p. 437 - 443 (2007/10/02)

The regioselective synthesis of isomeric 5(3)-aminomethyl-3(5)-phenyl isoxazoles using different methods is described. Spectroscopic data, especially mass spectrometric fragmentation, were used to identify and characterize the regioisomers. The muscarinic

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