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1034306-29-0

C16H24OSi is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1034306-29-0 Structure

  • Basic information

    1. Product Name: C16H24OSi
    2. Synonyms: C16H24OSi
    3. CAS NO:1034306-29-0
    4. Molecular Formula:
    5. Molecular Weight: 260.451
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1034306-29-0.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: C16H24OSi(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H24OSi(1034306-29-0)
    11. EPA Substance Registry System: C16H24OSi(1034306-29-0)

  • 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: 1034306-29-0(Hazardous Substances Data)

1034306-29-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1034306-29-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,4,3,0 and 6 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1034306-29:
(9*1)+(8*0)+(7*3)+(6*4)+(5*3)+(4*0)+(3*6)+(2*2)+(1*9)=100
100 % 10 = 0
So 1034306-29-0 is a valid CAS Registry Number.

1034306-29-0Downstream Products

1034306-29-0Relevant articles and documents

Study of the reaction of 1,1-bis(trimethylsilyl)-2-phenylethylene with some acyl chlorides in the presence of AlCl3

Safa, Kazem D.,Samani, Soleiman Paymard,Tofangdarzadeh, Shahin,Hassanpour, Akbar

, p. 2004 - 2008 (2008/09/19)

1,1-Bis(trimethylsilyl)-2-phenylethylene (1), which has been synthesized from the Peterson reaction between (Me3Si)3CLi and benzaldehyde, reacts with various acyl chlorides (RCOCl, R = Me, Et, iso-Pr, n-Bu, iso-Bu, iso-C5H11, PhCH2, PhCH2CH2) in the presence of AlCl3 to give α-silyl-α,β-unsaturated enones 3a-3h with high E stereoselectivity along with trans-α,β-unsaturated ketones 4a-4h. The enones 3 can be partially converted into the ketones 4 with an excess of AlCl3. Reaction of 1 with RCOCl, (R = Ph, CH3CH=CH) afforded only the ketones 4. Yields were dependent on time and the amounts of AlCl3 used.

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