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3,4-Diphenylisoxazol-5-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

52392-73-1

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52392-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 52392-73-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,3,9 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 52392-73:
(7*5)+(6*2)+(5*3)+(4*9)+(3*2)+(2*7)+(1*3)=121
121 % 10 = 1
So 52392-73-1 is a valid CAS Registry Number.

52392-73-1SDS

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 3,4-diphenyl-1,2-oxazol-5-amine

1.2 Other means of identification

Product number -
Other names 5-Isoxazolamine,3,4-diphenyl

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:52392-73-1 SDS

52392-73-1Relevant academic research and scientific papers

Hoveyda-Grubbs II Catalyst: A Useful Catalyst for One-Pot Visible-Light-Promoted Ring Contraction and Olefin Metathesis Reactions

Ge, Yun,Sun, Wangbin,Pei, Bingbing,Ding, Jia,Jiang, Yaojia,Loh, Teck-Peng

supporting information, p. 2774 - 2777 (2018/05/22)

A one-pot reaction to synthesize functionalized 2H-azirines through visible-light-mediated ring contraction and olefin metathesis of isoxazoles is described. Hoveyda-Grubbs II catalyst was found to function as a photocatalyst for these transformations, al

Efficient regioselective synthesis of 4- and 5-substituted isoxazoles under thermal and microwave conditions

Lasri, Jamal,Mukhopadhyay, Suman,Charmier, M. Adilia Januario

experimental part, p. 1385 - 1389 (2009/04/10)

(Chemical Equation Presented) The [2+3] cycloaddition reaction between nitrile oxides 2 and the captodative olefins 1 or the methyl crotonate derivatives 4 is regioselective and leads to the formation of the 5-substituted amino-isoxazole 3 or the 4-substi

A convenient synthesis of 4-alkyl-5-aminoisoxazoles

Bourbeau, Matthew P.,Rider, James T.

, p. 3679 - 3680 (2007/10/03)

A series of 4-alkyl-5-aminoisoxazoles have been synthesized in high yield by nucleophilic addition of lithiated alkyl nitriles to (α)-chlorooximes. The scope and limitations of this reaction were examined by varying the nature of the nitrile and chloride

Preparation de β-alcoxy acrylonitriles et d'amino-5 isoxazoles a partir d'α-cyano β-nitro-styrenes et -stilbenes

Colau, Roger,Viel, Claude

, p. 163 - 167 (2007/10/02)

Previously we have examined the action of amines on Z α-cyano β-nitrostilbenes (1).We now would like to report the results of our studies on the action of two other nucleophiles (alcohols and thiols) on these stilbenes derivatives.At room temperature in a

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