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Isoxazole, 3,5-bis(4-bromophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55368-74-6

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55368-74-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55368-74-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,3,6 and 8 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55368-74:
(7*5)+(6*5)+(5*3)+(4*6)+(3*8)+(2*7)+(1*4)=146
146 % 10 = 6
So 55368-74-6 is a valid CAS Registry Number.

55368-74-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-bis(4-bromophenyl)-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:55368-74-6 SDS

55368-74-6Relevant academic research and scientific papers

Nitrosylsulfuric acid as a tandem reagent in the synthesis of 3,5-diarylisoxazoles from 1,2-diarylcyclopropanes

Bondarenko,Komarov,Karetnikov,Nikolaeva,Zyk

, p. 1200 - 1203 (2019/07/15)

It was demonstrated that nitrosylsulfuric acid can be successfully used as a tandem nitrosating and oxidizing agent in the synthesis of 3,5-diarylisoxazoles from 1,2-diarylcyclopropanes. The reaction proceeds highly regioselectively in the case of symmetr

Nitrosylsulfuric acid as an oxidant in the synthesis of 3,5-diarylisoxazoles

Bondarenko,Komarov,Kuznetsova,Nikolaeva,Gavrilova, A. Yu.,Zyk

, p. 517 - 520 (2018/07/06)

By six examples, it was demonstrated that nitrosylsulfuric acid can be successfully used for oxidation of 3,5-diaryl-4,5-dihydroisoxazoles to the corresponding 3,5-diarylisoxazoles. If the starting isoxazolines contain the aromatic substituents activated towards electrophilic substitution, nitration of both newly formed isoxazole and substituted benzene rings occurred.

Expeditious preparation of isoxazoles from Δ2-isoxazolines as advanced intermediates for functional materials

Vilela, Guilherme D.,Da Rosa, Rafaela R.,Schneider, Paulo H.,Bechtold, Ivan H.,Eccher, Juliana,Merlo, Aloir A.

supporting information; experimental part, p. 6569 - 6572 (2012/01/03)

A collection of isoxazoles derivatives has been efficiently synthesized in three steps. The oximation reaction of aldehydes followed by nitrile oxide [3+2] 1,3-dipolar cycloaddition and MnO2-oxidation reaction furnished the title compounds which were purified by simple filtration on celite.

Synthesis and in vitro antiprotozoal activities of dicationic 3,5-diphenylisoxazoles

Patrick, Donald A.,Bakunov, Stanislav A.,Bakunova, Svetlana M.,Kumar, E.V.K. Suresh,Lombardy, Richard J.,Jones, Susan Kilgore,Bridges, Arlene S.,Zhirnov, Oksana,Hall, James Edwin,Wenzler, Tanja,Brun, Reto,Tidwell, Richard R.

, p. 2468 - 2485 (2008/02/03)

3,5-Bis(4-amidinophenyl)isoxazole (3) - an analogue of 2,5-bis(4- amidinophenyl)furan (furamidine) in which the central furan ring is replaced by isoxazole - and 42 novel analogues were prepared by two general synthetic pathways. The 43 isoxazole derivati

Organic light-emitting diodes and related hole transport compounds

-

Page/Page column 10, (2010/02/14)

New organic light-emitting diodes and related hole transport compounds and methods for fabrication, using siloxane self-assembly techniques.

REACTION OF 1,2-DIARYLCYCLOPROPANES WITH COPPER NITRATE IN ACETIC ANHYDRIDE AS A METHOD FOR THE SYNTHESIS OF 3,5-DIARYLISOXAZOLES

Sychkova, L. D.,Shabarov, Yu. S.

, p. 261 - 264 (2007/10/02)

In the reaction of 1,2-diarylcyclopropanes with copper nitrate in acetic anhydride the only reaction path leads to the formation of 3,5-diarylisoxazoles.The course of the transformation is affected significantly by the configuration of the initial cyclopr

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