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38380-63-1

3α-methyl-4-cyclohexene-1α-2α-dicarboxylic acid-1-methyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 38380-63-1 Structure

  • Basic information

    1. Product Name: 3α-methyl-4-cyclohexene-1α-2α-dicarboxylic acid-1-methyl ester
    2. Synonyms:
    3. CAS NO:38380-63-1
    4. Molecular Formula:
    5. Molecular Weight: 198.219
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 38380-63-1.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: 3α-methyl-4-cyclohexene-1α-2α-dicarboxylic acid-1-methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3α-methyl-4-cyclohexene-1α-2α-dicarboxylic acid-1-methyl ester(38380-63-1)
    11. EPA Substance Registry System: 3α-methyl-4-cyclohexene-1α-2α-dicarboxylic acid-1-methyl ester(38380-63-1)

  • 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: 38380-63-1(Hazardous Substances Data)

38380-63-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 38380-63-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,3,8 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 38380-63:
(7*3)+(6*8)+(5*3)+(4*8)+(3*0)+(2*6)+(1*3)=131
131 % 10 = 1
So 38380-63-1 is a valid CAS Registry Number.

38380-63-1Downstream Products

38380-63-1Relevant articles and documents

Enantioselective desymmetrization of meso-cyclic anhydrides catalyzed by hexahydro-1H-pyrrolo[1,2-c]imidazolones

Uozumi, Yasuhiro,Yasoshima, Kayo,Miyachi, Takamasa,Nagai, Shin-ichi

, p. 411 - 414 (2001)

Asymmetric methanolysis of meso cyclic carboxylic anhydrides including hexahydrophthalic anhydride proceeded in toluene in the presence of (6R,7aS)-(2-aryl-6-hydroxy)hexahydro-1H-pyrrolo[1,2-c]imidazol-1-one to give the corresponding desymmetrized mono ester acids (e.g. (1S,2R)-2-(methoxycarbonyl)cyclohexane-1-carboxylic acid) with enantiomeric excesses of up to 89%.

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