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120608-95-9

Diethyl-dithiocarbamic acid difluoromethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 120608-95-9 Structure

  • Basic information

    1. Product Name: Diethyl-dithiocarbamic acid difluoromethyl ester
    2. Synonyms: Diethyl-dithiocarbamic acid difluoromethyl ester
    3. CAS NO:120608-95-9
    4. Molecular Formula:
    5. Molecular Weight: 199.289
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 120608-95-9.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: Diethyl-dithiocarbamic acid difluoromethyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Diethyl-dithiocarbamic acid difluoromethyl ester(120608-95-9)
    11. EPA Substance Registry System: Diethyl-dithiocarbamic acid difluoromethyl ester(120608-95-9)

  • 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: 120608-95-9(Hazardous Substances Data)

120608-95-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120608-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,6,0 and 8 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 120608-95:
(8*1)+(7*2)+(6*0)+(5*6)+(4*0)+(3*8)+(2*9)+(1*5)=99
99 % 10 = 9
So 120608-95-9 is a valid CAS Registry Number.

120608-95-9Downstream Products

120608-95-9Relevant articles and documents

Perfluoro- and Polyfluorosulfonic Acids. 21. Synthesis of Difluoromethyl Esters Using Fluorosulfonyldifluoroacetic Acid as a Difluorocarbene Precursor

Chen, Qing-Yun,Wu, Sheng-Wen

, p. 3023 - 3027 (1989)

Difluoromethyl alkanoates 5 and fluorinated and nonfluorinated alkanesulfonates 9 were synthesized in moderate yields by the reaction of alkali metal salts of acids with fluorosulfonyldifluoroacetic acid (3) in acetonitrile under mild conditions.The presumed intermediate anion FO2SCF2CO2- generates CF2: by elimination of SO2, CO2, and F-.The esters are formed by insertion of CF2: into the O-H of the acid, whereas HCF3 is formed by the competing capture of F-.Organic acids can be used indirectly in the reaction in the presence of inorganic salts such as Na2SO4 and KCl, with comparable yields of difluoromethyl esters.

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