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2-dodec-11-enyloxirane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

69227-94-7

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69227-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69227-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,2 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 69227-94:
(7*6)+(6*9)+(5*2)+(4*2)+(3*7)+(2*9)+(1*4)=157
157 % 10 = 7
So 69227-94-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H26O/c1-2-3-4-5-6-7-8-9-10-11-12-14-13-15-14/h2,14H,1,3-13H2

69227-94-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-dodec-11-enyloxirane

1.2 Other means of identification

Product number -
Other names EINECS 273-929-4

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:69227-94-7 SDS

69227-94-7Upstream product

69227-94-7Relevant academic research and scientific papers

Oxidation of Organic Substrates by Molecular Oxygen/Aldehyde/ Heteropolyoxometalate System

Hamamoto, Masatoshi,Nakayama, Kouichi,Nishiyama, Yutaka,Ishii, Yasutaka

, p. 6421 - 6425 (2007/10/02)

Heteropolyoxometalate-catalyzed oxidations of organic compounds such as olefins and cyclic ketones with molecular oxygen in the presence of an aldehyde were examined.Olefins were epoxidized with dioxygen in the presence of 2 equiv of 2-methylpropanal under the influence of a catalytic amount of the mixed heteropolyoxometalate NPV6Mo6 (3) to give the corresponding epoxides in moderate to good yields.This catalytic oxidation method was also applied to the epoxidation of allylic and homoallylic alcohols.In the absence of olefins, the aldehydes were efficiently convertedinto the corresponding carboxylic acids.In addition, the Baeyer-Villiger oxidation of cyclic ketones was accomplished by using benzaldehyde instead of 2-methylpropanal as the aldehyde.

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