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960318-77-8

C20H28OSi is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 960318-77-8 Structure

  • Basic information

    1. Product Name: C20H28OSi
    2. Synonyms: C20H28OSi
    3. CAS NO:960318-77-8
    4. Molecular Formula:
    5. Molecular Weight: 312.527
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 960318-77-8.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: C20H28OSi(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H28OSi(960318-77-8)
    11. EPA Substance Registry System: C20H28OSi(960318-77-8)

  • 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: 960318-77-8(Hazardous Substances Data)

960318-77-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 960318-77-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,6,0,3,1 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 960318-77:
(8*9)+(7*6)+(6*0)+(5*3)+(4*1)+(3*8)+(2*7)+(1*7)=178
178 % 10 = 8
So 960318-77-8 is a valid CAS Registry Number.

960318-77-8Upstream product

960318-77-8Downstream Products

960318-77-8Relevant articles and documents

Rhodium-catalyzed asymmetric rearrangement of alkynyl alkenyl carbinols: Synthetic equivalent to asymmetric conjugate alkynylation of enones

Nishimura, Takahiro,Katoh, Taisuke,Takatsu, Keishi,Shintani, Ryo,Hayashi, Tamio

, p. 14158 - 14159 (2008/09/18)

Asymmetric 1,3-rearrangement of an alkynyl group of alkynyl alkenyl carbinols giving β-alkynylketones took place in high yields with high enantioselectivity in the presence of a hydroxyrhodium/(R)-binap catalyst. The present method including a key β-alkynyl elimination step in the catalytic cycle is synthetically equivalent to the asymmetric conjugate addition of terminal alkynes to β-substituted enones. Copyright

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