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937704-62-6

C8F14O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 937704-62-6 Structure

  • Basic information

    1. Product Name: C8F14O3S
    2. Synonyms:
    3. CAS NO:937704-62-6
    4. Molecular Formula:
    5. Molecular Weight: 442.13
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 937704-62-6.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: C8F14O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C8F14O3S(937704-62-6)
    11. EPA Substance Registry System: C8F14O3S(937704-62-6)

  • 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: 937704-62-6(Hazardous Substances Data)

937704-62-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 937704-62-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,7,7,0 and 4 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 937704-62:
(8*9)+(7*3)+(6*7)+(5*7)+(4*0)+(3*4)+(2*6)+(1*2)=196
196 % 10 = 6
So 937704-62-6 is a valid CAS Registry Number.

937704-62-6Relevant articles and documents

Functionalization of saturated fluorocarbons with and without light

Chen, Xudong,Lemal, David M.

, p. 1158 - 1167 (2006)

Photochemical transformation of saturated fluorocarbons into tetrabutylammonium enolates has been improved, and a method employing ketyls as reductants has been developed that accomplishes the same chemistry without light. Enolates have been isolated as enol methyl ethers, from which they can be efficiently regenerated with tetrabutylammonium iodide. In other cases, enolates have been isolated as the corresponding ketone or stable enol. Fluorocarbon LUMO energies correlate with their reactivity and serve as a guide to the choice of ketyl. Use of this chemistry for fluoropolymer surface modification is discussed.

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