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1239969-18-6

C19H22F2N2Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1239969-18-6 Structure

  • Basic information

    1. Product Name: C19H22F2N2Si
    2. Synonyms: C19H22F2N2Si
    3. CAS NO:1239969-18-6
    4. Molecular Formula:
    5. Molecular Weight: 344.479
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1239969-18-6.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: C19H22F2N2Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H22F2N2Si(1239969-18-6)
    11. EPA Substance Registry System: C19H22F2N2Si(1239969-18-6)

  • 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: 1239969-18-6(Hazardous Substances Data)

1239969-18-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1239969-18-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,9,9,6 and 9 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1239969-18:
(9*1)+(8*2)+(7*3)+(6*9)+(5*9)+(4*6)+(3*9)+(2*1)+(1*8)=206
206 % 10 = 6
So 1239969-18-6 is a valid CAS Registry Number.

1239969-18-6Downstream Products

1239969-18-6Relevant articles and documents

Selective propargylation of AZO compounds with barium reagents

Yanagisawa, Akira,Koide, Takanori,Yoshida, Kazuhiro

experimental part, p. 1515 - 1518 (2010/08/20)

A Barbier-type propargylation of azo compounds with γ- trialkylsilylated propargylic bromides has been achieved using reactive barium as a low-valent metal in THF. Corresponding propargylated hydrazines (α-adducts) were exclusively formed not only from azobenzenes (diaryldiazenes) but also from dialkyl azodicarboxylates. This method is also applicable to -alkylated or γ-phenylated propargylic bromides, providing the desired propargylated products only. Georg Thieme Verlag Stuttgart New York.

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