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1427321-54-7

7-[(tert-butyldiphenylsilyl)oxy]-1-(trimethylsilyl)hept-1-yn-3-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1427321-54-7 Structure

  • Basic information

    1. Product Name: 7-[(tert-butyldiphenylsilyl)oxy]-1-(trimethylsilyl)hept-1-yn-3-ol
    2. Synonyms: 7-[(tert-butyldiphenylsilyl)oxy]-1-(trimethylsilyl)hept-1-yn-3-ol
    3. CAS NO:1427321-54-7
    4. Molecular Formula:
    5. Molecular Weight: 438.758
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1427321-54-7.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: 7-[(tert-butyldiphenylsilyl)oxy]-1-(trimethylsilyl)hept-1-yn-3-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-[(tert-butyldiphenylsilyl)oxy]-1-(trimethylsilyl)hept-1-yn-3-ol(1427321-54-7)
    11. EPA Substance Registry System: 7-[(tert-butyldiphenylsilyl)oxy]-1-(trimethylsilyl)hept-1-yn-3-ol(1427321-54-7)

  • 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: 1427321-54-7(Hazardous Substances Data)

1427321-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1427321-54-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,3,2 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1427321-54:
(9*1)+(8*4)+(7*2)+(6*7)+(5*3)+(4*2)+(3*1)+(2*5)+(1*4)=137
137 % 10 = 7
So 1427321-54-7 is a valid CAS Registry Number.

1427321-54-7Relevant articles and documents

Synthesis of functionalized allenamides from ynamides by enolate claisen rearrangement

Brioche, Julien,Meyer, Christophe,Cossy, Janine

, p. 1626 - 1629 (2013)

The Claisen rearrangement of N-Boc glycinates derived from ynamido-alcohols affords an efficient and stereoselective access to highly functionalized allenamides. These compounds undergo silver-catalyzed cyclization to 3-pyrrolines which are useful precurs

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