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((Z)-2-Isocyanato-vinyl)-benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 60995-82-6 Structure
  • Basic information

    1. Product Name: ((Z)-2-Isocyanato-vinyl)-benzene
    2. Synonyms:
    3. CAS NO:60995-82-6
    4. Molecular Formula:
    5. Molecular Weight: 145.161
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 60995-82-6.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: ((Z)-2-Isocyanato-vinyl)-benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: ((Z)-2-Isocyanato-vinyl)-benzene(60995-82-6)
    11. EPA Substance Registry System: ((Z)-2-Isocyanato-vinyl)-benzene(60995-82-6)
  • 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: 60995-82-6(Hazardous Substances Data)

60995-82-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 60995-82-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,0,9,9 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 60995-82:
(7*6)+(6*0)+(5*9)+(4*9)+(3*5)+(2*8)+(1*2)=156
156 % 10 = 6
So 60995-82-6 is a valid CAS Registry Number.

60995-82-6Upstream product

60995-82-6Relevant articles and documents

Synthesis of Enamides

Brettle, Roger,Mosedale, Alan J.

, p. 2185 - 2196 (2007/10/02)

(Z)-3-Arylprop-2-enoic acids can be converted by the Curtius procedure, through the acyl azides, into (Z)-2-arylethenyl isocyanates, which with methanol give methyl (Z)-N-(2-arylethenyl)carbamates.Acylation of the (Z)-enecarbamates, through their anions, leads to methyl (Z)-N-acyl-N-(2-arylethenyl)carbamates, which on treatment with lithium iodide in boiling N,N-dimethylformamide or acetonitrile undergo demethoxycarbonylation to give (Z)-enamides.The stereospecific route to enamides can also be used in the E-series.Treatment of (Z)- or (E)-2-arylethenyl isocyanates with trifluoroacetic acid gives (E)-N-(2-arylethenyl)trifluoroacetamides,the anions of which, with acylating agents, give (E)-enamides directly.

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