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494748-15-1

Cyclohexanemethanol, a-methyl-, hydrogen sulfate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 494748-15-1 Structure

  • Basic information

    1. Product Name: Cyclohexanemethanol, a-methyl-, hydrogen sulfate
    2. Synonyms:
    3. CAS NO:494748-15-1
    4. Molecular Formula: C8H16O4S
    5. Molecular Weight: 208.279
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 494748-15-1.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: Cyclohexanemethanol, a-methyl-, hydrogen sulfate(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanemethanol, a-methyl-, hydrogen sulfate(494748-15-1)
    11. EPA Substance Registry System: Cyclohexanemethanol, a-methyl-, hydrogen sulfate(494748-15-1)

  • 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: 494748-15-1(Hazardous Substances Data)

494748-15-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 494748-15-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,4,7,4 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 494748-15:
(8*4)+(7*9)+(6*4)+(5*7)+(4*4)+(3*8)+(2*1)+(1*5)=201
201 % 10 = 1
So 494748-15-1 is a valid CAS Registry Number.

494748-15-1Upstream product

494748-15-1Relevant articles and documents

A stereoselective inverting sec -alkylsulfatase for the deracemization of sec -alcohols

Schober, Markus,Gadler, Petra,Knaus, Tanja,Kayer, Heidemarie,Birner-Gruenberger, Ruth,Guelly, Christian,MacHeroux, Peter,Wagner, Ulrike,Faber, Kurt

, p. 4296 - 4299 (2011)

A metallo-β-lactamase-type alkylsulfatase was found to catalyze the enantioselective hydrolysis of sec-alkylsulfates with strict inversion of configuration. This catalytic event, which does not have an analog in chemocatalysis, yields homochiral (S)-configurated alcohols and nonreacted sulfate esters. The latter could be converted into (S)-sec-alcohols as the sole product in up to >99% ee via a chemoenzymatic deracemization protocol on a preparative scale.

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