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91420-43-8

Ethanone, 1-[2-(trimethylsilyl)-3-benzofuranyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 91420-43-8 Structure

  • Basic information

    1. Product Name: Ethanone, 1-[2-(trimethylsilyl)-3-benzofuranyl]-
    2. Synonyms:
    3. CAS NO:91420-43-8
    4. Molecular Formula: C13H16O2Si
    5. Molecular Weight: 232.354
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91420-43-8.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: Ethanone, 1-[2-(trimethylsilyl)-3-benzofuranyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Ethanone, 1-[2-(trimethylsilyl)-3-benzofuranyl]-(91420-43-8)
    11. EPA Substance Registry System: Ethanone, 1-[2-(trimethylsilyl)-3-benzofuranyl]-(91420-43-8)

  • 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: 91420-43-8(Hazardous Substances Data)

91420-43-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91420-43-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,2 and 0 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91420-43:
(7*9)+(6*1)+(5*4)+(4*2)+(3*0)+(2*4)+(1*3)=108
108 % 10 = 8
So 91420-43-8 is a valid CAS Registry Number.

91420-43-8Downstream Products

91420-43-8Relevant articles and documents

AN EFFICIENT FRIEDEL-CRAFTS SYNTHESIS OF 2-ACYLBENZOFURANS

Gill, Melvyn

, p. 621 - 626 (1984)

2-(Trimethylsilyl)benzofuran, available quantitatively from benzofuran itself, reacts rapidly with primary, secondary, and tertiary aliphatic carboxylic acid chlorides in the presence of titanium(IV) chloride at low temperature to afford the corresponding 2-acylbenzofurans in excellent yields.This approach offers significant synthetic advantage over existing routes to the title compounds.

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