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28114-20-7

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28114-20-7 Usage

Synthesis Reference(s)

The Journal of Organic Chemistry, 58, p. 6421, 1993 DOI: 10.1021/jo00075a043Tetrahedron Letters, 27, p. 795, 1986 DOI: 10.1016/S0040-4039(00)84103-9

Check Digit Verification of cas no

The CAS Registry Mumber 28114-20-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,1,1 and 4 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 28114-20:
(7*2)+(6*8)+(5*1)+(4*1)+(3*4)+(2*2)+(1*0)=87
87 % 10 = 7
So 28114-20-7 is a valid CAS Registry Number.

28114-20-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-epoxyheptane

1.2 Other means of identification

Product number -
Other names 1,2-epoxynonane

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:28114-20-7 SDS

28114-20-7Relevant articles and documents

Copper based coordination polymers based on metalloligands: Utilization as heterogeneous oxidation catalysts

Kumar, Gulshan,Hussain, Firasat,Gupta, Rajeev

, p. 16985 - 16994 (2019/01/03)

This work presents the synthesis and characterization of two Cu(ii)-based coordination polymers prepared by utilizing two different Co(iii)-based metalloligands offering appended arylcarboxylic acid groups. Both coordination polymers are three-dimensional in nature and present pores and channels filled with water molecules. Both coordination polymers function as heterogeneous catalysts for the epoxidation of various olefins using O2 while employing isobutyraldehyde as the coreductor and for peroxide-mediated oxidation of assorted benzyl alcohols. The catalytic results illustrate efficient oxidation reactions, whereas the hot-fltration test and leaching experiments indicate the true heterogeneous nature of the catalysis.

Synthesis and Absolute Configuration of Two Natural Phenolic Homobenzyl Esters

Xu, Murong,Zhu, Shijun,Xu, Zejun,Wu, Yikang,Gao, Po

, p. 729 - 738 (2015/12/05)

Two recently identified natural phenolic homobenzyl esters, isolated from Phragmipedium calurum (an orchid) and Eupatorium fortunei TURCZ (a perennial herb in the Asteraceae family), respectively, were synthesized in enantiopure forms. By comparison of the optical rotations for the synthetic and the natural samples, the absolute configurations for the natural products were reliably assigned. The synthesis also enables establishment of the absolute configuration of a closely related natural homobenzyl alcohol and provided for the first time complete physical and spectroscopic data for two other natural homobenzyl esters. Two recently isolated natural phenolic homobenzyl esters were synthesized in enantiopure forms. The absolute configurations for these natural products were thus reliably assigned. En route to the total synthesis of the first target, complete physical and spectroscopic data for two other related natural products were made available for the first time. Configuration assignment of a third natural product was also achieved.

Formation of persulphate from sodium sulphite and molecular oxygen catalysed by H5PV2Mo10O40-aerobic epoxidation and hydrolysis

Rubinstein, Amir,Carmeli, Raanan,Neumann, Ronny

, p. 13247 - 13249 (2015/05/20)

The H5PV2Mo10O40 polyoxometalate catalysed the electron transfer oxidation of sulphite to yield a sulphite radical, SO3- that upon addition of O2 yielded a peroxosulphate species efficient for the H5PV2Mo10O40 catalysed epoxidation of alkenes. The acidic polyoxometalate further catalysed hydrolysis of the epoxide to give vicinal diols in high yields. This journal is

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