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2-Fluoro-5-phenyl-2-trimethylsilanyl-pentan-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124411-69-4 Structure
  • Basic information

    1. Product Name: 2-Fluoro-5-phenyl-2-trimethylsilanyl-pentan-1-ol
    2. Synonyms: 2-Fluoro-5-phenyl-2-trimethylsilanyl-pentan-1-ol
    3. CAS NO:124411-69-4
    4. Molecular Formula:
    5. Molecular Weight: 254.42
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124411-69-4.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: 2-Fluoro-5-phenyl-2-trimethylsilanyl-pentan-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Fluoro-5-phenyl-2-trimethylsilanyl-pentan-1-ol(124411-69-4)
    11. EPA Substance Registry System: 2-Fluoro-5-phenyl-2-trimethylsilanyl-pentan-1-ol(124411-69-4)
  • 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: 124411-69-4(Hazardous Substances Data)

124411-69-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124411-69-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,1 and 1 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124411-69:
(8*1)+(7*2)+(6*4)+(5*4)+(4*1)+(3*1)+(2*6)+(1*9)=94
94 % 10 = 4
So 124411-69-4 is a valid CAS Registry Number.

124411-69-4Relevant articles and documents

REGIOSPECIFIC RING OPENING OF α,β-EPOXYSILANES WITH SILICON TETRAFLUORIDE AND APPLICATION TO THE SYNTHESIS OF FLUOROALKENES

Shimizu, Makoto,Yoshioka, Hirosuke

, p. 967 - 970 (1989)

α,β-Epoxysilanes undergo the ring opening-fluorination with silicon tetrafluoride in the presence of diisopropylethylamine and water to give β-fluoro-β-silyl alcohols specifically, and the subsequent olefination with potassium hexamethyldisilazide affords fluoroalkenes in good yield.

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