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CAS

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321175-56-8

1-Phenyl-1-(trimethylsilyl)-2-propen-1-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 321175-56-8 Structure

  • Basic information

    1. Product Name: 1-Phenyl-1-(trimethylsilyl)-2-propen-1-ol
    2. Synonyms: 1-Phenyl-1-(trimethylsilyl)-2-propen-1-ol
    3. CAS NO:321175-56-8
    4. Molecular Formula:
    5. Molecular Weight: 206.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 321175-56-8.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: 1-Phenyl-1-(trimethylsilyl)-2-propen-1-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-Phenyl-1-(trimethylsilyl)-2-propen-1-ol(321175-56-8)
    11. EPA Substance Registry System: 1-Phenyl-1-(trimethylsilyl)-2-propen-1-ol(321175-56-8)

  • 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: 321175-56-8(Hazardous Substances Data)

321175-56-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 321175-56-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,1,1,7 and 5 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 321175-56:
(8*3)+(7*2)+(6*1)+(5*1)+(4*7)+(3*5)+(2*5)+(1*6)=108
108 % 10 = 8
So 321175-56-8 is a valid CAS Registry Number.

321175-56-8Relevant articles and documents

"Syn-Effect" in the Desilylation Reaction of γ-Silylated Allylic and Vinylic Sulfones

Guha, Samar Kumar,Ukaji, Yutaka,Inomata, Katsuhiko

, p. 1158 - 1159 (2003)

The desilylation reaction of γ-silylated allylic sulfones was found to proceed through γ-silylated (E)-vinylic sulfones to afford the corresponding allylic sulfones by treatment with DBU and H2O. The Z/ E ratio of the resulting allylic sulfones varied according to the γ-substituents of the γ-silylated sulfones. This stereo-chemical outcome was rationalized by "syn-effect".

Cerium(III) chloride-mediated vinylation of acylsilanes: A convenient new entry to silylated allylic alcohols

Bonini,Comes-Franchini,Fochi,Mazzanti,Ricci,Varchi

, p. 1688 - 1690 (2007/10/03)

The reaction of alkyl, cycloalkyl, aromatic, heteroaromatic and α,β-unsaturated acylsilanes 1-7 and of homochiral acylsilanes 15 and 16 with the complex vinylmagnesium bromide/CeCl3 affords the silylated allylic alcohols in satisfactory to exce

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