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5-CHLORO-3-(4-NITROPHENYL)ISOXAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

142598-83-2

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142598-83-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142598-83-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,5,9 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 142598-83:
(8*1)+(7*4)+(6*2)+(5*5)+(4*9)+(3*8)+(2*8)+(1*3)=152
152 % 10 = 2
So 142598-83-2 is a valid CAS Registry Number.

142598-83-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-3-(4-nitrophenyl)-1,2-oxazole

1.2 Other means of identification

Product number -
Other names -

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:142598-83-2 SDS

142598-83-2Relevant academic research and scientific papers

Nitration of 1,1-dihalo-2-(4'-nitrophenyl)cyclopropanes: New method to prepare isoxazole

Lin,Lin,Yao

, p. 3155 - 3156 (1992)

5-Halo-3-(4'-nitrophenyl)isoxazoles were prepared from the nitration of 1,1-dihalo-2-(4'-nitrophenyl)cyclopropanes in good yields.

Nitrosylsulfuric acid in the synthesis of 5-chloroisoxazoles from 1,1-dichlorocyclopropanes

Bondarenko, Oksana B.,Garaev, Zaur M.,Komarov, Arseniy I.,Kuznetsova, Lyubov I.,Gutorova, Svetlana V.,Skvortsov, Dmitry A.,Zyk, Nikolai V.

, p. 419 - 420 (2019/08/20)

Nitrosylsulfuric acid is shown to be a usable reagent for the synthesis of 5-chloroisoxazoles from readily available 1,1-di-chlorocyclopropanes via nitrosation–heterocyclization reaction. A cytotoxicity of some of the prepared 5-chloroisoxazoles towards M

Transformations of gem-dichloroarylcyclopropanes in the reaction with NOCl·2SO3. Synthesis of 3-aryl-5-chloroisoxazoles

Bondarenko,Gavrilova,Murodov,Zefirov,Zyk

, p. 186 - 194 (2013/07/25)

Nitrosation with complex NOCl·2SO3 of gem-dichloroarylcyclopropanes containing acceptor substituents in the aromatic ring proceeded chemo- and regioselectively affording 3-aryl-5-chloroisoxazoles in high yields. The presence of donor substituents complicated the reaction by the occurrence of competing processes.

Nitration of 2-Aryl-1,1-dichlorocyclopropanes

Lin, Shao-Tao,Yang, Fu-May

, p. 1554 - 1564 (2007/10/03)

A series of 2-aryl-1,1-dichlorocyclopropanes were nitrated with a mixture of nitric acid and sulfuric acid.The results suggest that an electron-withdrawing group on the phenyl ring and gem-dihalogens on the cyclopropane ring are essential for isoxazole formation.

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