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924715-43-5

N-(2-cyanophenyl)-O-phenylcarbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 924715-43-5 Structure

  • Basic information

    1. Product Name: N-(2-cyanophenyl)-O-phenylcarbamate
    2. Synonyms: N-(2-cyanophenyl)-O-phenylcarbamate
    3. CAS NO:924715-43-5
    4. Molecular Formula:
    5. Molecular Weight: 238.246
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 924715-43-5.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: N-(2-cyanophenyl)-O-phenylcarbamate(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(2-cyanophenyl)-O-phenylcarbamate(924715-43-5)
    11. EPA Substance Registry System: N-(2-cyanophenyl)-O-phenylcarbamate(924715-43-5)

  • 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: 924715-43-5(Hazardous Substances Data)

924715-43-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 924715-43-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,4,7,1 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 924715-43:
(8*9)+(7*2)+(6*4)+(5*7)+(4*1)+(3*5)+(2*4)+(1*3)=175
175 % 10 = 5
So 924715-43-5 is a valid CAS Registry Number.

924715-43-5Relevant articles and documents

Arylureas derived from colchicine: Enhancement of colchicine oncogene downregulation activity

Blasco, Víctor,Cu?at, Ana C.,Sanz-Cervera, Juan F.,Marco, J. Alberto,Falomir, Eva,Murga, Juan,Carda, Miguel

, p. 817 - 828 (2018)

Our efforts to get therapeutically useful colchicine derivatives for the treatment of cancer have led us to synthetize and biologically evaluate twenty-seven N,N′-disubstituted ureas containing a colchicine moiety and an aryl fragment. The cytotoxicity of

In situ generation and trapping of thioimidates: An intermolecular tandem reaction to 4-acylimino-4H-3,1-benzothiazines

Steinebach, Christian,Schulz-Fincke, Anna-Christina,Schnakenburg, Gregor,Gütschow, Michael

, p. 15430 - 15440 (2016/02/23)

The proton-catalyzed transformation of 2-thioureidobenzonitriles to 4-acylimino-4H-3,1-benzothiazines was accomplished by treatment with carboxylic anhydrides, acid chlorides or alkyl chloroformates. The reaction involves a cyclization to 4-imino-3,1-benz

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