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2-{[(3-phenylprop-2-yn-1-yl)oxy]methyl}oxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

42468-63-3

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42468-63-3 Usage

Alias

Allyl phenyl ether epoxide

Physical State

Colorless liquid

Uses

Production of polymers, solvent in pharmaceutical and chemical industries, cross-linking agent in coatings, adhesives, and sealants

Chemical Structure

Contains a three-membered ring with an oxygen atom (epoxide), making it reactive and versatile in synthesis reactions.

Check Digit Verification of cas no

The CAS Registry Mumber 42468-63-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,4,6 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 42468-63:
(7*4)+(6*2)+(5*4)+(4*6)+(3*8)+(2*6)+(1*3)=123
123 % 10 = 3
So 42468-63-3 is a valid CAS Registry Number.

42468-63-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-phenylprop-2-ynoxymethyl)oxirane

1.2 Other means of identification

Product number -
Other names (3-phenyl-prop-2-ynyloxymethyl)-oxirane

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:42468-63-3 SDS

42468-63-3Relevant academic research and scientific papers

Nickel-catalyzed reductive coupling of alkynes and epoxides

Molinaro, Carmela,Jamison, Timothy F.

, p. 8076 - 8077 (2007/10/03)

Nickel-catalyzed, intramolecular and intermolecular reductive coupling of alkynes and epoxides affords synthetically useful homoallylic alcohols of defined alkene geometry. Very high regioselectivity is generally observed, and cyclizations proceed with complete selectivity for endo epoxide opening. This catalytic reaction represents the first use of a non-π-based electrophile in a growing class of nickel-catalyzed, multicomponent coupling reactions, and is the first catalytic method of reductive coupling of alkynes and epoxides that is effective for both intermolecular and intramolecular cases, and mechanistically distinct from these, possibly involving a nickella(II)oxetane. Copyright

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