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535921-03-0

3-acetyl-4-[2-(4-bromo-phenyl)-2-oxo-ethylamino]-chromen-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 535921-03-0 Structure

  • Basic information

    1. Product Name: 3-acetyl-4-[2-(4-bromo-phenyl)-2-oxo-ethylamino]-chromen-2-one
    2. Synonyms:
    3. CAS NO:535921-03-0
    4. Molecular Formula:
    5. Molecular Weight: 400.228
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 535921-03-0.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-acetyl-4-[2-(4-bromo-phenyl)-2-oxo-ethylamino]-chromen-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-acetyl-4-[2-(4-bromo-phenyl)-2-oxo-ethylamino]-chromen-2-one(535921-03-0)
    11. EPA Substance Registry System: 3-acetyl-4-[2-(4-bromo-phenyl)-2-oxo-ethylamino]-chromen-2-one(535921-03-0)

  • 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: 535921-03-0(Hazardous Substances Data)

535921-03-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 535921-03-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,3,5,9,2 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 535921-03:
(8*5)+(7*3)+(6*5)+(5*9)+(4*2)+(3*1)+(2*0)+(1*3)=150
150 % 10 = 0
So 535921-03-0 is a valid CAS Registry Number.

535921-03-0Relevant articles and documents

Efficient synthesis of trisubstituted [1]benzopyrano[4,3-b]pyrrol-4(1H)-one derivatives from 4-hydroxycoumarin

Liao, Yuan-Xiu,Kuo, Pei-Yu,Yang, Ding-Yah

, p. 1599 - 1602 (2003)

Various trisubstituted [1]benzopyrano[4,3-b]pyrrol-4(1H)-one derivatives have been synthesized from 4-hydroxycoumarin with a 30-40% yield over six steps. The key step of the synthesis is a base-promoted intramolecular cyclization of enamines 5, followed by dehydration to generate the fused pyrrole ring.

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