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14774-55-1

3-Furancarbonitrile, 2-amino-4-(4-methylphenyl)-5-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 14774-55-1 Structure

  • Basic information

    1. Product Name: 3-Furancarbonitrile, 2-amino-4-(4-methylphenyl)-5-phenyl-
    2. Synonyms:
    3. CAS NO:14774-55-1
    4. Molecular Formula: C18H14N2O
    5. Molecular Weight: 274.322
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14774-55-1.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: 3-Furancarbonitrile, 2-amino-4-(4-methylphenyl)-5-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-Furancarbonitrile, 2-amino-4-(4-methylphenyl)-5-phenyl-(14774-55-1)
    11. EPA Substance Registry System: 3-Furancarbonitrile, 2-amino-4-(4-methylphenyl)-5-phenyl-(14774-55-1)

  • 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: 14774-55-1(Hazardous Substances Data)

14774-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14774-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,7 and 4 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 14774-55:
(7*1)+(6*4)+(5*7)+(4*7)+(3*4)+(2*5)+(1*5)=121
121 % 10 = 1
So 14774-55-1 is a valid CAS Registry Number.

14774-55-1Upstream product

14774-55-1Relevant articles and documents

Ring Transformation and Reactions of 2-Amino-4,5-dihydrofuran-3,4-dicarbonitriles

Aran, Vincente J.,Perez, Miguel A.,Soto, Jose L.

, p. 2009 - 2011 (1984)

The 2-amino-4,5-dihydrofuran-3,4-dicarbonitriles (1a-f) were thermally aromatized to the 2-aminofuran-3-carbonitriles (2a-f) which, in turn, underwent photoxidative ring transformation into the 2,5-dihydro-5-hydroxy-2-oxopyrrole-3-carbonitriles (3b-e).Mil

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