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(4-but-3-enyl-phenoxy)-tert-butyl-dimethyl-silane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 459867-15-3 Structure
  • Basic information

    1. Product Name: (4-but-3-enyl-phenoxy)-tert-butyl-dimethyl-silane
    2. Synonyms: (4-but-3-enyl-phenoxy)-tert-butyl-dimethyl-silane
    3. CAS NO:459867-15-3
    4. Molecular Formula:
    5. Molecular Weight: 262.467
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 459867-15-3.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: (4-but-3-enyl-phenoxy)-tert-butyl-dimethyl-silane(CAS DataBase Reference)
    10. NIST Chemistry Reference: (4-but-3-enyl-phenoxy)-tert-butyl-dimethyl-silane(459867-15-3)
    11. EPA Substance Registry System: (4-but-3-enyl-phenoxy)-tert-butyl-dimethyl-silane(459867-15-3)
  • 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: 459867-15-3(Hazardous Substances Data)

459867-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 459867-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,9,8,6 and 7 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 459867-15:
(8*4)+(7*5)+(6*9)+(5*8)+(4*6)+(3*7)+(2*1)+(1*5)=213
213 % 10 = 3
So 459867-15-3 is a valid CAS Registry Number.

459867-15-3Relevant articles and documents

Effect of ligand structure on the zinc-catalyzed Henry reaction. Asymmetric syntheses of (-)-denopamine and (-)-arbutamine

Trost, Barry M.,Yeh, Vince S. C.,Ito, Hisanako,Bremeyer, Nadine

, p. 2621 - 2623 (2007/10/03)

(Matrix presented) Syntheses of variously modified ligands for the dinuclear zinc catalysts for the asymmetric aldol and nitroaldol (Henry) reactions are reported. Catalytic enantioselective nitroaldol reactions promoted by these modified ligands led to efficient syntheses of the β-preceptor agonists (-)-denopamine and (-)-arbutamine.

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