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(4R)-1-(1-hydroxy-1-methylethyl)-4-methylcyclohexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 24302-23-6 Structure
  • Basic information

    1. Product Name: (4R)-1-(1-hydroxy-1-methylethyl)-4-methylcyclohexene
    2. Synonyms: (4R)-1-(1-hydroxy-1-methylethyl)-4-methylcyclohexene
    3. CAS NO:24302-23-6
    4. Molecular Formula:
    5. Molecular Weight: 154.252
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24302-23-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (4R)-1-(1-hydroxy-1-methylethyl)-4-methylcyclohexene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4R)-1-(1-hydroxy-1-methylethyl)-4-methylcyclohexene(24302-23-6)
    11. EPA Substance Registry System: (4R)-1-(1-hydroxy-1-methylethyl)-4-methylcyclohexene(24302-23-6)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 24302-23-6(Hazardous Substances Data)

24302-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24302-23-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,0 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24302-23:
(7*2)+(6*4)+(5*3)+(4*0)+(3*2)+(2*2)+(1*3)=66
66 % 10 = 6
So 24302-23-6 is a valid CAS Registry Number.

24302-23-6Relevant articles and documents

An efficient procedure for the 1,3-transposition of allylic alcohols based on lithium naphthalenide induced reductive elimination of epoxy mesylates

Wu, Yen-Ku,Liu, Hsing-Jang,Zhu, Jia-Liang

, p. 621 - 623 (2008/12/22)

An efficient protocol for the 1,3-transposition of allylic alcohols has been developed. The method is based on the pretransformation of allylic alcohols into the corresponding epoxy mesylates, followed by the reductive elimination of the resulting epoxy mesylates by using lithium naphthalenide (LN) as a reducing agent. Georg Thieme Verlag Stuttgart.

Lipase-catalyzed resolution of p-menthan-3-ols monoterpenes: Preparation of the enantiomer-enriched forms of menthol, isopulegol, trans- and cis-piperitol, and cis-isopiperitenol

Serra, Stefano,Brenna, Elisabetta,Fuganti, Claudio,Maggioni, Francesco

, p. 3313 - 3319 (2007/10/03)

A study on the enzymic resolution of the most common p-menthan-3-ol monoterpene isomers is described. Enantioenriched alcohols 1, 5, 10, 11 and 12 are obtained by means of the lipase-mediated kinetic acetylation of the corresponding racemic materials. The stereochemical aspects of the enzymic process have been investigated. We found that the structural features of the starting p-menthan-3-ol as well as the kind of lipase used, impacted strongly on the enantioselectivity of the resolution. The potentialities of this approach for preparative purposes are discussed.

A convergent synthesis of the spiroketal moiety of the HIV-1 protease inhibitors didemnaketals

Jia, Yan Xing,Li, Xin,Wu, Bin,Zhao, Xue Zhi,Tu, Yong Qiang

, p. 1697 - 1708 (2007/10/03)

The stereoselective synthesis of the spiroketal fragment 4a and its C1″-epimer 4b of the HIV-1 protease inhibitors didemnaketals has been carried out through multisteps from the natural (R)-(+)-pulegone, which involved the diastereoselective construction of four chiral carbon centers by intramolecular chiral induction.

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