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C21H28N2O2Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1239969-17-5 Structure
  • Basic information

    1. Product Name: C21H28N2O2Si
    2. Synonyms:
    3. CAS NO:1239969-17-5
    4. Molecular Formula:
    5. Molecular Weight: 368.551
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1239969-17-5.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: C21H28N2O2Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H28N2O2Si(1239969-17-5)
    11. EPA Substance Registry System: C21H28N2O2Si(1239969-17-5)
  • 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: 1239969-17-5(Hazardous Substances Data)

1239969-17-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1239969-17-5 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 1239969-17:
(9*1)+(8*2)+(7*3)+(6*9)+(5*9)+(4*6)+(3*9)+(2*1)+(1*7)=205
205 % 10 = 5
So 1239969-17-5 is a valid CAS Registry Number.

1239969-17-5Downstream Products

1239969-17-5Relevant articles and documents

Selective propargylation of AZO compounds with barium reagents

Yanagisawa, Akira,Koide, Takanori,Yoshida, Kazuhiro

, p. 1515 - 1518 (2010)

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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