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911710-57-1

2-[3-(tert-butyl-diphenyl-silanyloxy)-prop-1-ynyl]-furan-3-carbaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 911710-57-1 Structure

  • Basic information

    1. Product Name: 2-[3-(tert-butyl-diphenyl-silanyloxy)-prop-1-ynyl]-furan-3-carbaldehyde
    2. Synonyms: 2-[3-(tert-butyl-diphenyl-silanyloxy)-prop-1-ynyl]-furan-3-carbaldehyde
    3. CAS NO:911710-57-1
    4. Molecular Formula:
    5. Molecular Weight: 388.538
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 911710-57-1.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: 2-[3-(tert-butyl-diphenyl-silanyloxy)-prop-1-ynyl]-furan-3-carbaldehyde(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[3-(tert-butyl-diphenyl-silanyloxy)-prop-1-ynyl]-furan-3-carbaldehyde(911710-57-1)
    11. EPA Substance Registry System: 2-[3-(tert-butyl-diphenyl-silanyloxy)-prop-1-ynyl]-furan-3-carbaldehyde(911710-57-1)

  • 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: 911710-57-1(Hazardous Substances Data)

911710-57-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 911710-57-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,7,1 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 911710-57:
(8*9)+(7*1)+(6*1)+(5*7)+(4*1)+(3*0)+(2*5)+(1*7)=141
141 % 10 = 1
So 911710-57-1 is a valid CAS Registry Number.

911710-57-1Relevant articles and documents

Intermolecular [4 + 2] cycloaddition of o-quinodimethanes derived from ene-bis(sulfinylallenes)

Kitagaki, Shinji,Katoh, Kumiko,Ohdachi, Kazuhiro,Takahashi, Yuji,Shibata, Daisuke,Mukai, Chisato

, p. 6908 - 6914 (2007/10/03)

Intermolecular [4 + 2] cycloaddition of o-quinodimethanes, prepared in situ from ene-bis(propargyl alcohols) and benzenesulfenyl chloride via ene-bis(sulfinylallene) formation, was investigated. Benzene-bridged bis(propargyl alcohols) reacted with both el

Rh(I)-catalyzed allenic Pauson-Khand reaction: First construction of the bicyclo[6.3.0]undecadienone ring system

Mukai, Chisato,Hirose, Toshiyuki,Teramoto, Satoshi,Kitagaki, Shinji

, p. 10983 - 10994 (2007/10/03)

The Rh(I)-catalyzed Pauson-Khand reaction of allenynes afforded the bicyclo[6.3.0]undecadienones as well as their benzo and furo derivatives. In addition, a novel [RhCl(CO)2]2-catalyzed [2,3]-sigmatropic rearrangement of the sulfinic

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