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80909-78-0

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80909-78-0 Usage

General Description

2-(4-bromophenyl)-2-methyloxirane is a chemical compound with the molecular formula C9H9BrO. It is commonly used as a reagent in organic synthesis and is known for its ability to undergo ring-opening reactions with various nucleophiles. The compound contains a bromine atom and a phenyl group attached to a two-carbon oxirane ring, giving it a unique combination of reactivity and potential applications. It is important to handle this compound with care, as it is classified as a hazardous material and should only be used by trained professionals in a controlled laboratory setting.

Check Digit Verification of cas no

The CAS Registry Mumber 80909-78-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,9,0 and 9 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80909-78:
(7*8)+(6*0)+(5*9)+(4*0)+(3*9)+(2*7)+(1*8)=150
150 % 10 = 0
So 80909-78-0 is a valid CAS Registry Number.

80909-78-0SDS

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 2-(4-bromophenyl)-2-methyloxirane

1.2 Other means of identification

Product number -
Other names 1,2-epoxy-2-(4-bromophenyl)propane

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:80909-78-0 SDS

80909-78-0Relevant articles and documents

Chemical space exploration of oxetanes

Cou?ago, Rafael M.,Laufer, Stefan,de Sá Alves, Fernando Rodrigues

, p. 1 - 18 (2020/11/05)

This paper focuses on new derivatives bearing an oxetane group to extend accessible chemical space for further identification of kinase inhibitors. The ability to modulate kinase activity represents an important therapeutic strategy for the treatment of h

Retro-Corey-Chaykovsky Epoxidation: Converting Geminal Disubstituted Epoxides to Ketones

Li, Siqi,Li, Pingfan,Xu, Jiaxi

, (2019/09/13)

Corey-Chaykovsky epoxidation has been widely applied in the conversion of aldehydes and ketones to epoxides with sulfonium and sulfoxonium ylides. The reverse transformation is realized for conversion of geminal disubstituted epoxides to ketones in the presence of DABCO in refluxing mesitylene. The method is a weak basic transformation from epoxides to ketones with loss of a methylene group and can be applied as an alternative strategy of the acid-catalyzed Meinwald rearrangement or oxidation for conversion of epoxides to carbonyl compounds.

SUBSTITUTED 2-[PHENOXY-PHENYL]-1-[1,2,4]TRIAZOL-1-YL-ETHANOL COMPOUNDS AND THEIR USE AS FUNGICIDES

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Page/Page column 84, (2014/06/23)

The present invention relates to substituted 2-[phenoxy-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds of formula I as defined in the description,and the N-oxides, and salts thereof, their preparation and intermediates for preparing them. The invention also relates to the use of these compounds for combating harmful fungi and seed coated with at least one such compound and also to compositions comprising at least one such compound.

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