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129265-05-0

1-Fluoro-1-phenyl-2-methoxy-2-(phenylthio)ethene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 129265-05-0 Structure

  • Basic information

    1. Product Name: 1-Fluoro-1-phenyl-2-methoxy-2-(phenylthio)ethene
    2. Synonyms: 1-Fluoro-1-phenyl-2-methoxy-2-(phenylthio)ethene
    3. CAS NO:129265-05-0
    4. Molecular Formula:
    5. Molecular Weight: 260.332
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 129265-05-0.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: 1-Fluoro-1-phenyl-2-methoxy-2-(phenylthio)ethene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Fluoro-1-phenyl-2-methoxy-2-(phenylthio)ethene(129265-05-0)
    11. EPA Substance Registry System: 1-Fluoro-1-phenyl-2-methoxy-2-(phenylthio)ethene(129265-05-0)

  • 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: 129265-05-0(Hazardous Substances Data)

129265-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 129265-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,2,6 and 5 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 129265-05:
(8*1)+(7*2)+(6*9)+(5*2)+(4*6)+(3*5)+(2*0)+(1*5)=130
130 % 10 = 0
So 129265-05-0 is a valid CAS Registry Number.

129265-05-0Relevant articles and documents

Electrolytic Reactions of Fluoro Organic Compounds. 7. Anodic Methoxylation and Acetoxylation of 2,2,2-Trifluoroethyl Sulfides. Preparation of Highly Useful Trifluoromethylated Building Blocks

Fuchigami, Toshio,Yamamoto, Kayoko,Nakagawa, Yuki

, p. 137 - 142 (2007/10/02)

Anodic methoxylation and acetoxylation of 2,2,2-trifluoroethyl sulfides and the corresponding nonfluorinated sulfides were comparatively studied.It was found that a trifluoromethyl group remarkably promoted anodic substitution and methoxy and acetoxy groups were introduced adjacent to the trifluoromethyl group of the sulfides.Longer perfluoroalkyl groups also promoted these anodic substitutions.These products were shown to be highly useful building blocks fro the synthesis of fluoro organic compounds.

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