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219325-59-4

3-AMINO-3-[1,1'-BIPHENYL]-4-YL-2-PROPENOIC ACID ETHYL ESTER is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 219325-59-4 Structure

  • Basic information

    1. Product Name: 3-AMINO-3-[1,1'-BIPHENYL]-4-YL-2-PROPENOIC ACID ETHYL ESTER
    2. Synonyms: 3-AMINO-3-[1,1'-BIPHENYL]-4-YL-2-PROPENOIC ACID ETHYL ESTER
    3. CAS NO:219325-59-4
    4. Molecular Formula: C17H17NO2
    5. Molecular Weight: 267.326
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 219325-59-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-AMINO-3-[1,1'-BIPHENYL]-4-YL-2-PROPENOIC ACID ETHYL ESTER(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-AMINO-3-[1,1'-BIPHENYL]-4-YL-2-PROPENOIC ACID ETHYL ESTER(219325-59-4)
    11. EPA Substance Registry System: 3-AMINO-3-[1,1'-BIPHENYL]-4-YL-2-PROPENOIC ACID ETHYL ESTER(219325-59-4)

  • 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: 219325-59-4(Hazardous Substances Data)

219325-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219325-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,3,2 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 219325-59:
(8*2)+(7*1)+(6*9)+(5*3)+(4*2)+(3*5)+(2*5)+(1*9)=134
134 % 10 = 4
So 219325-59-4 is a valid CAS Registry Number.

219325-59-4Downstream Products

219325-59-4Relevant articles and documents

Indolequinone antitumor agents: Correlation between quinone structure, rate of metabolism by recombinant human NAD(P)H:quinone oxidoreductase, and in vitro cytotoxicity

Beall, Howard D.,Winski, Shannon,Swann, Elizabeth,Hudnott, Anna R.,Cotterill, Ann S.,O'Sullivan, Noeleen,Green, Stephen J.,Bien, Richard,Siegel, David,Ross, David,Moody, Christopher J.

, p. 4755 - 4766 (2007/10/03)

A series of indolequinones bearing various functional groups has been synthesized, and the effects of substituents on the metabolism of the quinones by recombinant human NAD(P)H: quinone oxidoreductase (NQO1) were studied. Thus 5-methoxyindolequinones wer

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