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1042712-14-0

C13H17NO4Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1042712-14-0 Structure

  • Basic information

    1. Product Name: C13H17NO4Si
    2. Synonyms: C13H17NO4Si
    3. CAS NO:1042712-14-0
    4. Molecular Formula:
    5. Molecular Weight: 279.368
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1042712-14-0.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: C13H17NO4Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13H17NO4Si(1042712-14-0)
    11. EPA Substance Registry System: C13H17NO4Si(1042712-14-0)

  • 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: 1042712-14-0(Hazardous Substances Data)

1042712-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1042712-14-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,2,7,1 and 2 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1042712-14:
(9*1)+(8*0)+(7*4)+(6*2)+(5*7)+(4*1)+(3*2)+(2*1)+(1*4)=100
100 % 10 = 0
So 1042712-14-0 is a valid CAS Registry Number.

1042712-14-0Downstream Products

1042712-14-0Relevant articles and documents

Synthesis of functionalized 6(5H)-phenanthridinones based on a [3+3]-cyclocondensation/lactamization strategy

Yawer, Mirza A.,Hussain, Ibrar,Iqbal, Inam,Spannenberg, Anke,Langer, Peter

, p. 4467 - 4469 (2008)

Functionalized 6(5H)-phenanthridinones (dibenzo[b,d]pyrid-6-ones) were prepared by [3+3]-cyclocondensation of 1-trimethylsilyloxy-1,3-butadienes with nitro-substituted 1-aryl-1-silyloxy-1-en-3-ones and subsequent reductive lactamization.

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