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4-[(5-phenylisoxazol-3-yl)methyl]morpholine is a complex organic compound with the molecular formula C14H16N2O2. It features a morpholine ring, which is a six-membered heterocyclic compound containing two nitrogen atoms and four carbon atoms. The compound is characterized by a 5-phenylisoxazol-3-yl group attached to the morpholine ring through a methylene bridge. The phenyl group in the isoxazole ring provides additional structural complexity and potential for various chemical interactions. 4-[(5-phenylisoxazol-3-yl)methyl]morpholine may have applications in pharmaceuticals, agrochemicals, or as a building block in the synthesis of more complex molecules due to its unique structure and potential reactivity.

1026-63-7

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1026-63-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1026-63-7 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 3 respectively.
Calculate Digit Verification of CAS Registry Number 1026-63:
(6*1)+(5*0)+(4*2)+(3*6)+(2*6)+(1*3)=47
47 % 10 = 7
So 1026-63-7 is a valid CAS Registry Number.

1026-63-7Downstream Products

1026-63-7Relevant academic research and scientific papers

Synthesis of functional isoxazole derivatives proceeding from (5-arylisoxazol-3-yl)chloromethanes

Potkin,Bumagin,Petkevich,Dikusar,Semenova,Kurman,Zolotar',Pashkevich,Gurinovich,Kul'Chitskii

, p. 1119 - 1130 (2015/10/12)

Reaction of 3-chloromethyl-5-phenyl(p-tolyl)isoxazoles with substituted phenols under the conditions of Williamson reaction afforded the corresponding 3-aryloxymethyl-5-phenyl(p-tolyl)isoxazoles. Treating the latter with sodium methylate, sodium phenyl(benzyl, furfuryl)thiolates and morpholine in methanol resulted in the replacement of the chlorine atom in 3-chloromethyl-5-phenyl(p-tolyl)isoxazoles by methoxy-, phenyl-(benzyl, furfuryl)sulfanyl groups and morpholine residue.

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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