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103615-39-0

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103615-39-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103615-39-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,3,6,1 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 103615-39:
(8*1)+(7*0)+(6*3)+(5*6)+(4*1)+(3*5)+(2*3)+(1*9)=90
90 % 10 = 0
So 103615-39-0 is a valid CAS Registry Number.

103615-39-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name (1R,2R,5R,1'S)-5-methyl-2-(1'-methyloxiranyl)cyclohexanol

1.2 Other means of identification

Product number -
Other names (1R,2R,5R)-5-Methyl-2-((S)-2-methyl-oxiranyl)-cyclohexanol

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:103615-39-0 SDS

103615-39-0Relevant articles and documents

Stereoselective synthesis and application of isopulegol-based bi- And trifunctional chiral compounds

Endre, Gábor,Fül?p, Ferenc,Huynh, Thu,Le, Tam Minh,Szakonyi, Zsolt,Szekeres, András

, p. 38468 - 38477 (2020)

A new family of isopulegol-based bi- and trifunctional chiral ligands was developed from commercially available (-)-isopulegol. Nucleophilic addition of primary amines towards (+)-α-methylene-γ-butyrolactone was accomplished, followed by reduction of the

Sustainable catalytic epoxidation of biorenewable terpene feedstocks using H2O2as an oxidant in flow microreactors

Bull, Steven D.,Cunningham, William B.,Plucinski, Pawel,Tibbetts, Joshua D.,Vezzoli, Massimiliano

supporting information, p. 5449 - 5455 (2021/08/16)

Solvent-free continuous flow epoxidation of the alkene bonds of a range of biorenewable terpene substrates have been carried out using a recyclable tungsten-based polyoxometalate phase transfer catalyst and aqueous H2O2 as a benign oxidant. These sustainable flow epoxidation reactions are carried out in commercial microreactors containing static mixing channels that enable common monoterpenes (e.g. untreated crude sulfate turpentine, limonene, etc.) to be safely epoxidized in short reaction times and in good yields. These flow procedures are applicable for the flow epoxidation of trisubstituted and disubstituted alkenes for the safe production of multigram quantities of a wide range of epoxides. This journal is

Novel multicomponent oxidation catalyst and process for producing epoxy compound therewith

-

Page/Page column 4/1-2, (2008/06/13)

A novel multicomponent oxidation catalyst that can be effectively used in, for example, an epoxidation reaction of olefins, etc., being inexpensive and high in versatility and that exhibits high catalytic activity; and a process for producing an epoxy com

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