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Cyclohexanol, 5-methyl-2-[(2R)-2-methyloxiranyl]-, (1R,2R,5R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

103615-41-4

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103615-41-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 103615-41-4 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, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 103615-41:
(8*1)+(7*0)+(6*3)+(5*6)+(4*1)+(3*5)+(2*4)+(1*1)=84
84 % 10 = 4
So 103615-41-4 is a valid CAS Registry Number.

103615-41-4SDS

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'R)-5-methyl-2-(1'-methyloxiranyl)cyclohexanol

1.2 Other means of identification

Product number -
Other names (1R,2R,5R)-5-Methyl-2-((R)-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:103615-41-4 SDS

103615-41-4Relevant articles and documents

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

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 (2020/11/05)

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 protocols for the solvent free epoxidation and: Anti -dihydroxylation of the alkene bonds of biorenewable terpene feedstocks using H2O2 as oxidant

Cunningham, William B.,Tibbetts, Joshua D.,Hutchby, Marc,Maltby, Katarzyna A.,Davidson, Matthew G.,Hintermair, Ulrich,Plucinski, Pawel,Bull, Steven D.

supporting information, p. 513 - 524 (2020/02/13)

A tungsten-based polyoxometalate catalyst employing aqueous H2O2 as a benign oxidant has been used for the solvent free catalytic epoxidation of the trisubstituted alkene bonds of a wide range of biorenewable terpene substrates. This epoxidation protocol has been scaled up to produce limonene oxide, 3-carene oxide and α-pinene oxide on a multigram scale, with the catalyst being recycled three times to produce 3-carene oxide. Epoxidation of the less reactive disubstituted alkene bonds of terpene substrates could be achieved by carrying out catalytic epoxidation reactions at 50 °C. Methods have been developed that enable direct epoxidation of untreated crude sulfate turpentine to afford 3-carene oxide, α-pinene oxide and β-pinene oxide. Treatment of crude epoxide products (no work-up) with a heterogeneous acid catalyst (Amberlyst-15) results in clean epoxide hydrolysis to afford their corresponding terpene-anti-diols in good yields.

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

Synthetic studies of the HIV-1 protease inhibitive didemnaketals: Stereocontrolled synthesis of an ester side chain

Zhao, Xue Zhi,Tu, Yong Qiang,Peng, Lei,Li, Xue Qiang,Jia, Yan Xing

, p. 3713 - 3716 (2007/10/03)

The stereocontrolled synthesis of the C1-C8 portion, the ester side chain of the HIV-1 protease inhibitive didemnaketals from the ascidian Didemnum sp., has been carried out through 15 steps starting from (S)-carvone as the chiral template. This approach involved the diastereoselective construction of three conjoint chiral centers by intramolecular chiral inducement, and generation of allylic alcohol intermediate through a key Grob fragmentation reaction.

A facile synthesis of (6S,1′S)-(+)-hernandulcin and (6S,1′R)-(+)-epihernandulcin

Kim, Jung Hun,Lim, Hyun Jin,Cheon, Seung Hoon

, p. 7501 - 7507 (2007/10/03)

A facile total synthesis of (+)-hernandulcin (1) was accomplished from (-)-isopulegol in 6 steps with 15% overall yield. Epoxidation of (-)-isopulegol with m-chloroperbenzoic acid followed by opening of the epoxide 3a with prenyl Grignard afforded the tertiary alcohol 4a with correct C-6 and C-1′ stereochemistry as a major product. Oxidation of the secondary alcohol in compound 4a to the ketone 5a was accomplished in high yield by using TPAP and N-methylmorpholine N-oxide. Conversion of the ketone 5a to α,β -unsaturated ketone via organoselenium intermediate gave (+)-hernandulcin (1). This method was also successfully applied to the synthesis of (+)-epihernandulcin (2).

Synthesis of (+)-hernandulcin and (+)-epihernandulcin

Kim, Jung Hun,Lim, Hyun Jin,Cheon, Seung Hoon

, p. 4721 - 4722 (2007/10/03)

(+)-Hernandulcin 1, an extremely sweet bisabolane-type sesquiterpene, and (+)-epihernandulcin 2 were synthesized in six steps from (-)-isopulegol with 15 and 11 percent overall yields, respectively.

A simple and efficient protocol for epoxidation of olefins using dimethyldioxirane

Ferraz, Helena M. C.,Muzzi, Rozanna M.,De O. Vieira, Tiago,Viertler, Hans

, p. 5021 - 5023 (2007/10/03)

The reaction of a series of monoterpenic olefins and Δ4-octalins with dimethyldioxirane led to the corresponding epoxides in excellent yields. Remarkable diastereoselectivity was observed for the Δ4-octalins. The procedure consists simply in stirring the substrate, NaHCO3 and acetone, at 0°C, with dropwise addition of an aqueous solution of oxone. (C) 2000 Elsevier Science Ltd.

TOTAL SYNTHESIS OF VARIOUS ELEMANOLIDES

Friedrich, Dirk,Bohlmann, Ferdinand

, p. 1369 - 1392 (2007/10/02)

Starting with a suitable substituted divinyl cyclohexanone, eleven naturally occurring 12.8-elemanolides bearing exo-methylene or methyl groups at C-11 and differing in substitution as well as in relative configuration, have been synthesized in racemic form.An approach to elemanolides with additional oxygen functionalities is principally possible by modification of the basic concept.Methods for the oxidative generation of terpenoid exo-methylene lactone and furan units are exemplified by synthesis of menthofuran and the p-menthenolides from isopulegols.

Synthesis of menthofuran

-

, (2008/06/13)

A new process for synthesizing menthofuran is disclosed. Said process comprises epoxidizing isopulegol to form the new compound isopulegol epoxide. The epoxide is then oxidized to form isopulegone epoxide which can be cyclodehydrated to form menthofuran.

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