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1228279-12-6

C29H43N3OSi is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1228279-12-6 Structure

  • Basic information

    1. Product Name: C29H43N3OSi
    2. Synonyms: C29H43N3OSi
    3. CAS NO:1228279-12-6
    4. Molecular Formula:
    5. Molecular Weight: 477.765
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1228279-12-6.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: C29H43N3OSi(CAS DataBase Reference)
    10. NIST Chemistry Reference: C29H43N3OSi(1228279-12-6)
    11. EPA Substance Registry System: C29H43N3OSi(1228279-12-6)

  • 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: 1228279-12-6(Hazardous Substances Data)

1228279-12-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1228279-12-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,8,2,7 and 9 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1228279-12:
(9*1)+(8*2)+(7*2)+(6*8)+(5*2)+(4*7)+(3*9)+(2*1)+(1*2)=156
156 % 10 = 6
So 1228279-12-6 is a valid CAS Registry Number.

1228279-12-6Upstream product

1228279-12-6Downstream Products

1228279-12-6Relevant articles and documents

Activation of ammonia by a Si - O double bond and formation of a unique pair of sila-hemiaminal and silanoic amide tautomers

Xiong, Yun,Yao, Shenglai,Mueller, Robert,Kaupp, Martin,Driess, Matthias

, p. 6912 - 6913 (2010)

The new silanone complex 3 is accessible in 82% yield and is capable of undergoing addition of ammonia under mild conditions, yielding the sila-hemiaminal 4 and, at the same time, its unique tautomer 5, the first silanoic amide. The unexpected formation of 3 is due to the presence of the basic exocyclic methylene group in the C3N2 ligand backbone. Strikingly, the tautomers 4 and 5 are in equilibrium in solution and can be cocrystallized in benzene or THF solutions having a SiOH...O Si hydrogen bond as confirmed by single-crystal X-ray diffraction analysis.

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