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CAS

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131750-34-0

Methanesulfonic acid (S)-cyclohexyl-((2S,3S)-3-cyclohexyl-oxiranyl)-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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  • 131750-34-0 Structure

  • Basic information

    1. Product Name: Methanesulfonic acid (S)-cyclohexyl-((2S,3S)-3-cyclohexyl-oxiranyl)-methyl ester
    2. Synonyms:
    3. CAS NO:131750-34-0
    4. Molecular Formula:
    5. Molecular Weight: 316.462
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 131750-34-0.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: Methanesulfonic acid (S)-cyclohexyl-((2S,3S)-3-cyclohexyl-oxiranyl)-methyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Methanesulfonic acid (S)-cyclohexyl-((2S,3S)-3-cyclohexyl-oxiranyl)-methyl ester(131750-34-0)
    11. EPA Substance Registry System: Methanesulfonic acid (S)-cyclohexyl-((2S,3S)-3-cyclohexyl-oxiranyl)-methyl ester(131750-34-0)

  • 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: 131750-34-0(Hazardous Substances Data)

131750-34-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 131750-34-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,7,5 and 0 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 131750-34:
(8*1)+(7*3)+(6*1)+(5*7)+(4*5)+(3*0)+(2*3)+(1*4)=100
100 % 10 = 0
So 131750-34-0 is a valid CAS Registry Number.

131750-34-0Relevant articles and documents

Telluride-mediated stereospecific conversion of racemic E-allylic alcohols to homochiral Z-allylic alcohols; transposition of primary and secondary allylic alcohols via glycidol derivatives

Discordia, Robert P.,Murphy, Christopher K.,Dittmer, Donald C.

, p. 5603 - 5606 (1990)

Racemic trans-secondary allylic alcohols can be converted to homochiral cis-secondary allylic alcohols by means of a telluride-mediated transposition reaction applied to the homochiral glycidol obtained from a Sharpless kinetic resolution. (+)-Linalool is obtained in>95% enantiomeric excess from geraniol, an example of a transposition of a primary allylic alcohol to a homochiral tertiary alcohol.

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