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1453477-52-5

C18H18N2O4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1453477-52-5 Structure

  • Basic information

    1. Product Name: C18H18N2O4
    2. Synonyms:
    3. CAS NO:1453477-52-5
    4. Molecular Formula:
    5. Molecular Weight: 326.352
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1453477-52-5.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: C18H18N2O4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C18H18N2O4(1453477-52-5)
    11. EPA Substance Registry System: C18H18N2O4(1453477-52-5)

  • 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: 1453477-52-5(Hazardous Substances Data)

1453477-52-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1453477-52-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,3,4,7 and 7 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1453477-52:
(9*1)+(8*4)+(7*5)+(6*3)+(5*4)+(4*7)+(3*7)+(2*5)+(1*2)=175
175 % 10 = 5
So 1453477-52-5 is a valid CAS Registry Number.

1453477-52-5Upstream product

1453477-52-5Downstream Products

1453477-52-5Relevant articles and documents

A Concise Synthesis of Pyrazole Analogues of CombretastatinA1 as Potent Anti-Tubulin Agents

Zaninetti, Roberta,Cortese, Salvatore V.,Aprile, Silvio,Massarotti, Alberto,Canonico, Pier Luigi,Sorba, Giovanni,Grosa, Giorgio,Genazzani, Armando A.,Pirali, Tracey

, p. 633 - 643 (2013)

CombretastatinA1 (CA1) binds to the β-subunit at the colchicine binding site of tubulin and inhibits polymerization. As such, it is both an antitumor agent and a vascular disrupting agent. It has been shown to be at least tenfold more potent than combreta

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