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32017-76-8

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32017-76-8 Usage

General Description

2-(4-Bromophenyl)oxirane, also known as 4-Bromo-2-phenyloxirane, is a chemical compound with the molecular formula C8H7BrO. It belongs to the oxirane class of compounds and contains a bromine atom and a phenyl group attached to a three-membered epoxide ring. 2-(4-BROMOPHENYL)OXIRANE is commonly used as a starting material in organic synthesis for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. It is also used as an intermediate in the production of polymers and other industrial materials. 2-(4-Bromophenyl)oxirane is considered to be a hazardous chemical and proper safety precautions should be followed when handling and using it.

Check Digit Verification of cas no

The CAS Registry Mumber 32017-76-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,2,0,1 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 32017-76:
(7*3)+(6*2)+(5*0)+(4*1)+(3*7)+(2*7)+(1*6)=78
78 % 10 = 8
So 32017-76-8 is a valid CAS Registry Number.
InChI:InChI=1/C8H7BrO/c9-7-3-1-6(2-4-7)8-5-10-8/h1-4,8H,5H2

32017-76-8 Well-known Company Product Price

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  • Alfa Aesar

  • (H26818)  (±)-4-Bromostyrene oxide, 98%   

  • 32017-76-8

  • 5g

  • 939.0CNY

  • Detail
  • Alfa Aesar

  • (H26818)  (±)-4-Bromostyrene oxide, 98%   

  • 32017-76-8

  • 25g

  • 2961.0CNY

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  • Aldrich

  • (534749)  2-(4-Bromophenyl)oxirane  96%

  • 32017-76-8

  • 534749-5G

  • 1,031.94CNY

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32017-76-8SDS

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 2-(4-BROMOPHENYL)OXIRANE

1.2 Other means of identification

Product number -
Other names Oxirane,(4-bromophenyl)

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:32017-76-8 SDS

32017-76-8Relevant articles and documents

Mechanochemical Synthesis of 1,2-Diketoindolizine Derivatives from Indolizines and Epoxides Using Piezoelectric Materials

Wang, Yumei,Zhang, Ziwu,Deng, Lichan,Lao, Tianfeng,Su, Zhengquan,Yu, Yue,Cao, Hua

supporting information, p. 7171 - 7176 (2021/09/14)

A simple and efficient mechanochemical-induced approach for the synthesis of 1,2-diketoindolizine derivatives has been developed. BaTiO3 was used as the piezoelectric material in this transformation. This method features no usage of solvent, simple experimental operation, scalable potential, and high conversion efficiency, which make it attractive and practical.

TAU-PROTEIN TARGETING COMPOUNDS AND ASSOCIATED METHODS OF USE

-

Paragraph 0350, (2021/02/12)

The present disclosure relates to bifunctional compounds, which find utility as modulators of tan protein. In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a VHL or cereblon ligand which binds to the E3 ubiquitin ligase and on the other end a moiety which binds tan protein, such that tan protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of tan. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of tan protein. Diseases or disorders that result from aggregation or accumulation of tan protein are treated or prevented with compounds and compositions of the present disclosure.

MeOTf/KI-catalyzed efficient synthesis of 2-arylnaphthalenesviacyclodimerization of styrene oxides

Chen, Chao,Xi, Chanjuan,Zhang, Zeyu,Zou, Song

supporting information, p. 8559 - 8565 (2021/10/20)

The MeOTf/KI-catalyzed synthesis of 2-arylnaphthalene derivatives from aryl ethylene oxides in alcohol under ambient conditions is described. The present protocol has a higher atom efficiency and wider substrate applicability with excellent yields. The reaction proceeded using the aryl ethylene oxides to give 2-arylnaphthalenes either in homo-coupling or in cross-coupling. The reaction could also be carried out at the gram scale in minutes.

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