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Isoxazole, 5-ethenyl-3-phenyl-, also known as 5-vinyl-3-phenylisoxazole, is an organic compound with the chemical formula C10H9NO. It is a heterocyclic compound, specifically a five-membered ring containing one oxygen atom and one nitrogen atom. Isoxazole, 5-ethenyl-3-phenyl- is characterized by the presence of a vinyl group (C=CH2) at the 5-position and a phenyl group (C6H5) at the 3-position. It is a colorless to pale yellow solid and is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. The compound is relatively stable and can be stored under standard conditions, but it should be handled with care due to its potential reactivity with strong acids, bases, and oxidizing agents.

5592-17-6

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5592-17-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5592-17-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,9 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5592-17:
(6*5)+(5*5)+(4*9)+(3*2)+(2*1)+(1*7)=106
106 % 10 = 6
So 5592-17-6 is a valid CAS Registry Number.

5592-17-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-5-vinylisoxazole

1.2 Other means of identification

Product number -
Other names 3-Phenyl-5-vinylisoxazol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5592-17-6 SDS

5592-17-6Relevant academic research and scientific papers

Polystyrene-supported 2-bromoallyl sulfone as an efficient reagent for synthesis of 3,5-disubstituted isoxazoles

Zhang, Liang,Mao, Xue-Chun,Wang, Qiu-Ying,Pan, Yang,Chen, Jun-Min

, p. 142 - 148 (2019/08/26)

A facile method has been developed for the solid-phase organic synthesis of 3,5-disubstituted isoxazoles from polystyrene-supported 2-bromoallyl sulfone. The advantages of this method include a straightforward and convenient procedure, high product yield,

General Platform for the Conversion of Isoxazol-5-ones to 3,5-Disubstituted Isoxazoles via Nucleophilic Substitutions and Palladium Catalyzed Cross-Coupling Strategies

Fernandes, Alessandra A. G.,da Silva, Amanda F.,Okada, Celso Y.,Suzukawa, Vitor,Cormanich, Rodrigo A.,Jurberg, Igor D.

, p. 3022 - 3034 (2019/05/17)

A general platform for the conversion of isoxazol-5-ones to 3,5-disubstituted isoxazoles has been developed via a two-step strategy. The first step leads to the formation of 5-(pseudo)halogenated isoxazoles, while in the second, a variety of heteroalkyl-, heteroaryl-, alkyl-, alkenyl-, alkynyl- and aryl-chains can be installed via nucleophilic substitutions or palladium catalyzed cross-coupling reactions.

3-aryl-5-vinyl-2-isoxazolines and 3-aryl-5-vinylisoxazoles from aryl nitrile oxides and methyl vinyl ketone lithium enolate: Reaction limits and synthetic utility exploitation

Salomone, Antonio,Scilimati, Antonio,Vitale, Paola

, (2015/02/02)

3-Aryl-5-hydroxy-5-vinyl-2-isoxazolines were synthesized by reacting aryl nitrile oxides with the lithium enolate of methyl vinyl ketone (MVK) at -78 °C. Fair to good yields are obtained in the case of aryl nitrile oxides bearing electron-withdrawing grou

5-Hydroxy-3-phenyl-5-vinyl-2-isoxazoline and 3-phenyl-5-vinylisoxazole: Synthesis and reactivity

Di Nunno, Leonardo,Scilimati, Antonio,Vitale, Paola

, p. 11270 - 11278 (2007/10/03)

5-Hydroxy-3-phenyl-5-vinyl-2-isoxazoline has been synthesized by reacting benzonitrile oxide with the enolate ion of methyl vinyl ketone. From 5-hydroxy-5-vinyl-2-isoxazoline, 5-vinylisoxazole was then quantitatively obtained by dehydration-aromatization

1,3-Dipolar cycloaddition of nitrile oxides to 1-phenylsulfonyl-1,3-butadienes: Synthesis of 3-(4,5-dihydroisoxazol-5-yl)pyrroles

Hwang, Sung Hee,Kurth, Mark J

, p. 53 - 56 (2007/10/03)

Novel heterocyclic compounds containing the 3-(4,5-dihydroisoxazol-5-yl)pyrrole ring system were synthesized in good yields (66-78%) by regioselective 1,3-dipolar cycloaddition of nitrile oxides to 1-phenylsulfonyl-1,3-dienes followed by Barton-Zard pyrrole annulation.

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