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868761-01-7

Silane, [difluoro(phenylseleno)methyl]trimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 868761-01-7 Structure

  • Basic information

    1. Product Name: Silane, [difluoro(phenylseleno)methyl]trimethyl-
    2. Synonyms:
    3. CAS NO:868761-01-7
    4. Molecular Formula: C10H14F2SeSi
    5. Molecular Weight: 279.263
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 868761-01-7.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: Silane, [difluoro(phenylseleno)methyl]trimethyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Silane, [difluoro(phenylseleno)methyl]trimethyl-(868761-01-7)
    11. EPA Substance Registry System: Silane, [difluoro(phenylseleno)methyl]trimethyl-(868761-01-7)

  • 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: 868761-01-7(Hazardous Substances Data)

868761-01-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 868761-01-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,8,7,6 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 868761-01:
(8*8)+(7*6)+(6*8)+(5*7)+(4*6)+(3*1)+(2*0)+(1*1)=217
217 % 10 = 7
So 868761-01-7 is a valid CAS Registry Number.

868761-01-7Relevant articles and documents

Synthesis and transformation of [difluoro(phenylseleno)methyl]- trimethylsilane

Qin, Ying-Ying,Qiu, Xiao-Long,Yang, Yan-Yan,Meng, Wei-Dong,Qing, Feng-Ling

, p. 9040 - 9043 (2005)

A novel and efficient strategy was developed to synthesize [difluoro(phenylseleno)methyl]trimethylsilane (PhSeCF2-TMS, 2), which was further utilized as a nucleophilic difluoromethylating reagent to incorporate the difluoro-(phenylseleno)methyl (PhSeCF2) group into carbonyl compounds in good yields. The resulting PhSeCF2-containing alcohols 3 could be conveniently converted into corresponding difluoromethyl alcohols 4 by a radical deselenylation.

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