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CAS

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854016-59-4

N-(phenyl-phenylimino-methyl)-benzamidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 854016-59-4 Structure

  • Basic information

    1. Product Name: N-(phenyl-phenylimino-methyl)-benzamidine
    2. Synonyms: N-(phenyl-phenylimino-methyl)-benzamidine
    3. CAS NO:854016-59-4
    4. Molecular Formula:
    5. Molecular Weight: 299.375
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 854016-59-4.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-(phenyl-phenylimino-methyl)-benzamidine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(phenyl-phenylimino-methyl)-benzamidine(854016-59-4)
    11. EPA Substance Registry System: N-(phenyl-phenylimino-methyl)-benzamidine(854016-59-4)

  • 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: 854016-59-4(Hazardous Substances Data)

854016-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 854016-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,4,0,1 and 6 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 854016-59:
(8*8)+(7*5)+(6*4)+(5*0)+(4*1)+(3*6)+(2*5)+(1*9)=164
164 % 10 = 4
So 854016-59-4 is a valid CAS Registry Number.

854016-59-4Relevant articles and documents

1,3,5-Triazapenta-1,3-dienes: Useful building blocks for the synthesis of 1,2-dihydro-1,3,5-triazines and oligonitriles

Hesse, Nadine,Froehlich, Roland,Wibbeling, Birgit,Wuerthwein, Ernst-Ulrich

, p. 3923 - 3937 (2007/10/03)

1,3,5-Triazapentadienes 1, prepared from amidines and imidoyl chlorides 2, have been used as nucleophilic building blocks for the reactions with various electrophilic reagents. With aldehydes 4 1,2-dihydrotriazines 3 were obtained, whereas ketones 5 gave

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