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1321619-34-4

C16H26O2Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1321619-34-4 Structure

  • Basic information

    1. Product Name: C16H26O2Si
    2. Synonyms: C16H26O2Si
    3. CAS NO:1321619-34-4
    4. Molecular Formula:
    5. Molecular Weight: 278.467
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1321619-34-4.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: C16H26O2Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H26O2Si(1321619-34-4)
    11. EPA Substance Registry System: C16H26O2Si(1321619-34-4)

  • 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: 1321619-34-4(Hazardous Substances Data)

1321619-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1321619-34-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,1,6,1 and 9 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1321619-34:
(9*1)+(8*3)+(7*2)+(6*1)+(5*6)+(4*1)+(3*9)+(2*3)+(1*4)=124
124 % 10 = 4
So 1321619-34-4 is a valid CAS Registry Number.

1321619-34-4Relevant articles and documents

Metal-free, aerobic dioxygenation of alkenes using simple hydroxamic acid derivatives

Giglio, Benjamin C.,Schmidt, Valerie A.,Alexanian, Erik J.

, p. 13320 - 13322 (2011)

The dioxygenation of alkenes using molecular oxygen and a simple hydroxamic acid derivative has been achieved. The reaction system consists of readily prepared methyl N-hydroxy-N-phenylcarbamate and molecular oxygen with a radical initiator, offering an alternative to common dioxygenation processes catalyzed by precious transition metals. This transformation capitalizes on the unique reactivity profile of hydroxamic acid derivatives in radical-mediated alkene addition processes.

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