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CAS

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1388859-18-4

(5-fluoro-2-(2-(4-(trifluoromethyl)phenyl)ethynyl)phenyl)diphenylsilanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1388859-18-4 Structure

  • Basic information

    1. Product Name: (5-fluoro-2-(2-(4-(trifluoromethyl)phenyl)ethynyl)phenyl)diphenylsilanol
    2. Synonyms: (5-fluoro-2-(2-(4-(trifluoromethyl)phenyl)ethynyl)phenyl)diphenylsilanol
    3. CAS NO:1388859-18-4
    4. Molecular Formula:
    5. Molecular Weight: 462.518
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1388859-18-4.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: (5-fluoro-2-(2-(4-(trifluoromethyl)phenyl)ethynyl)phenyl)diphenylsilanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (5-fluoro-2-(2-(4-(trifluoromethyl)phenyl)ethynyl)phenyl)diphenylsilanol(1388859-18-4)
    11. EPA Substance Registry System: (5-fluoro-2-(2-(4-(trifluoromethyl)phenyl)ethynyl)phenyl)diphenylsilanol(1388859-18-4)

  • 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: 1388859-18-4(Hazardous Substances Data)

1388859-18-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1388859-18-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,8,8,5 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1388859-18:
(9*1)+(8*3)+(7*8)+(6*8)+(5*8)+(4*5)+(3*9)+(2*1)+(1*8)=234
234 % 10 = 4
So 1388859-18-4 is a valid CAS Registry Number.

1388859-18-4Relevant articles and documents

Gold-catalyzed hydrosilyloxylation driving tandem aldol and Mannich reactions

Kang, Dongjin,Park, Sangjune,Ryu, Taekyu,Lee, Phil Ho

, p. 3912 - 3915 (2012/09/22)

The chemoselective formation of an enolate from alkyne in the presence of a carbonyl and imine group was realized, which constructed a variety of structural motifs under exceedingly mild reaction conditions in a tandem process. Reaction driving tandem hyd

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