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101067-64-5

<1-phenyl-1-(trimethylsiloxy)ethyl>-2-benzaldimine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 101067-64-5 Structure

  • Basic information

    1. Product Name: <1-phenyl-1-(trimethylsiloxy)ethyl>-2-benzaldimine
    2. Synonyms:
    3. CAS NO:101067-64-5
    4. Molecular Formula:
    5. Molecular Weight: 297.472
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 101067-64-5.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-(trimethylsiloxy)ethyl>-2-benzaldimine(CAS DataBase Reference)
    10. NIST Chemistry Reference: <1-phenyl-1-(trimethylsiloxy)ethyl>-2-benzaldimine(101067-64-5)
    11. EPA Substance Registry System: <1-phenyl-1-(trimethylsiloxy)ethyl>-2-benzaldimine(101067-64-5)

  • 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: 101067-64-5(Hazardous Substances Data)

101067-64-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 101067-64-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,0,6 and 7 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 101067-64:
(8*1)+(7*0)+(6*1)+(5*0)+(4*6)+(3*7)+(2*6)+(1*4)=75
75 % 10 = 5
So 101067-64-5 is a valid CAS Registry Number.

101067-64-5Relevant articles and documents

Synthesis of β-lactams from acetic acids and imines induced by phenyl dichlorophosphate reagent

Arrieta,Cossio,Palomo

, p. 1703 - 1712 (2007/10/02)

The development of a practical method for the preparation of vinylamino-β-lactams from Dane salts and Schiff bases is described. Among the reagents known to produce β-lactams from imines and acetic acids, only phenyl dichlorophosphate and 1-methyl-2-chloropyridinium iodide are suitable for the synthesis of vinylamino-β-lactams. Reaction of acetic acids with ethanolimine derivatives promoted by phenyl dichlorophosphate affords oxazolidines instead of β-lactams. Protection of the hydroxyl group as the trimethylsilyl ether in the starting Schiff bases provides a convenient route to the corresponding β-lactams instead of oxazolidines. Some observations on the scope of the method are made.

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