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326598-92-9

all-cis-3,5-dihydroxy-4-methyl-1-(methoxycarbonyl)cyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 326598-92-9 Structure

  • Basic information

    1. Product Name: all-cis-3,5-dihydroxy-4-methyl-1-(methoxycarbonyl)cyclohexane
    2. Synonyms: all-cis-3,5-dihydroxy-4-methyl-1-(methoxycarbonyl)cyclohexane
    3. CAS NO:326598-92-9
    4. Molecular Formula:
    5. Molecular Weight: 188.224
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 326598-92-9.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: all-cis-3,5-dihydroxy-4-methyl-1-(methoxycarbonyl)cyclohexane(CAS DataBase Reference)
    10. NIST Chemistry Reference: all-cis-3,5-dihydroxy-4-methyl-1-(methoxycarbonyl)cyclohexane(326598-92-9)
    11. EPA Substance Registry System: all-cis-3,5-dihydroxy-4-methyl-1-(methoxycarbonyl)cyclohexane(326598-92-9)

  • 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: 326598-92-9(Hazardous Substances Data)

326598-92-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 326598-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,6,5,9 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 326598-92:
(8*3)+(7*2)+(6*6)+(5*5)+(4*9)+(3*8)+(2*9)+(1*2)=179
179 % 10 = 9
So 326598-92-9 is a valid CAS Registry Number.

326598-92-9Relevant articles and documents

Asymmetrization of all-cis-3,5-dihydroxy-1-(methoxycarbonyl)cyclohexane and of the 4-methyl and 4-ethyl substituted homologues

Zhao, Yurui,Wu, Yusheng,De Clercq, Pierre,Vandewalle, Maurits,Maillos, Philippe,Pascal, Jean-Claude

, p. 3887 - 3900 (2000)

Enantiomerically pure mono acylated derivatives of cis,cis-3,5-dihydroxy-1-(methoxycarbonyl)cyclohexane 1, all-cis-3,5-dihydroxy-4-methyl-1-(methoxycarbonyl)cyclohexane 2 and all-cis-3,5-dihydroxy-4-ethyl-1-(methoxycarbonyl)cyclohexane 3 were obtained upon lipase catalyzed asymmetrization. PPL-catalyzed transesterification of 1 with vinyl acetate led in high yield to the (S)-monoacetate (+)-13. With substrates 2 and 3 this process was slower and gave the (R)-monoacetates (-)-14 and (-)-15; the best results were obtained with SAM II lipase. On the other hand, enantiotoposelective hydrolysis of their diacetates and especially dibutyrates gave useful results only for the 4-substituted substrates and produced the (S)-monoesters. Copyright (C) 2000 Elsevier Science Ltd.

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