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1429033-68-0

C37H45F3O6Si is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1429033-68-0 Structure

  • Basic information

    1. Product Name: C37H45F3O6Si
    2. Synonyms: C37H45F3O6Si
    3. CAS NO:1429033-68-0
    4. Molecular Formula:
    5. Molecular Weight: 670.841
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1429033-68-0.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: C37H45F3O6Si(CAS DataBase Reference)
    10. NIST Chemistry Reference: C37H45F3O6Si(1429033-68-0)
    11. EPA Substance Registry System: C37H45F3O6Si(1429033-68-0)

  • 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: 1429033-68-0(Hazardous Substances Data)

1429033-68-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1429033-68-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,9,0,3 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1429033-68:
(9*1)+(8*4)+(7*2)+(6*9)+(5*0)+(4*3)+(3*3)+(2*6)+(1*8)=150
150 % 10 = 0
So 1429033-68-0 is a valid CAS Registry Number.

1429033-68-0Downstream Products

1429033-68-0Relevant articles and documents

A stereoconvergent intramolecular Diels-Alder cycloaddition related to the construction of the decalin core of neo-clerodane diterpenoids

Butler, Sean C.,Forsyth, Craig J.

, p. 3895 - 3907 (2013/05/22)

Several examples of a highly specific, stereoconvergent intramolecular Diels-Alder cycloaddition that led to the trans-decalin core of neo-clerodane diterpenoids are described. The relative configuration adjacent to the dienophile, which led to C4 of the decalin system, as well as the electron-withdrawing effects of various substituents and conformational rigidity of the Diels-Alder precursors were explored.

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