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887266-68-4

N-benzyl-N-(trimethylsilanylethynyl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 887266-68-4 Structure

  • Basic information

    1. Product Name: N-benzyl-N-(trimethylsilanylethynyl)acetamide
    2. Synonyms: N-benzyl-N-(trimethylsilanylethynyl)acetamide
    3. CAS NO:887266-68-4
    4. Molecular Formula:
    5. Molecular Weight: 245.396
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 887266-68-4.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: N-benzyl-N-(trimethylsilanylethynyl)acetamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzyl-N-(trimethylsilanylethynyl)acetamide(887266-68-4)
    11. EPA Substance Registry System: N-benzyl-N-(trimethylsilanylethynyl)acetamide(887266-68-4)

  • 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: 887266-68-4(Hazardous Substances Data)

887266-68-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 887266-68-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,2,6 and 6 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 887266-68:
(8*8)+(7*8)+(6*7)+(5*2)+(4*6)+(3*6)+(2*6)+(1*8)=234
234 % 10 = 4
So 887266-68-4 is a valid CAS Registry Number.

887266-68-4Downstream Products

887266-68-4Relevant articles and documents

Enantioselective synthesis of axially chiral anilides through rhodium-catalyzed [2+2+2] cycloaddition of 1,6-diynes with trimethylsilylynamides

Tanaka, Ken,Takeishi, Kenzo,Noguchi, Keiichi

, p. 4586 - 4587 (2006)

We have developed a rhodium-catalyzed enantioselective intermolecular [2+2+2] cycloaddition of 1,6-diynes with trimethylsilylynamides for the synthesis of axially chiral anilides. The axial chirality is constructed at the formation of benzene rings with h

Preparation of enantioenriched axially chiral anilides via [2+2+2] cycloaddition of 1,6-diynes with trimethylsilylynamides

Tanaka, Ken,Takeishi, Kenzo

, p. 2920 - 2923 (2008/03/13)

The rhodium-catalyzed enantioselective [2+2+2] cycloaddition of 1,6-diynes with teimethylsilylynamides provides enantioenriched axially chiral anilides in poor to good yields with good to excellent enantioselectivity. Trimethylsilylynamides can be readily

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