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463358-39-6

4H-1-Benzopyran-4-one, 6-bromo-2-(4-methoxyphenyl)-, oxime is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 463358-39-6 Structure

  • Basic information

    1. Product Name: 4H-1-Benzopyran-4-one, 6-bromo-2-(4-methoxyphenyl)-, oxime
    2. Synonyms:
    3. CAS NO:463358-39-6
    4. Molecular Formula: C16H12BrNO3
    5. Molecular Weight: 346.18
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 463358-39-6.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: 4H-1-Benzopyran-4-one, 6-bromo-2-(4-methoxyphenyl)-, oxime(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4H-1-Benzopyran-4-one, 6-bromo-2-(4-methoxyphenyl)-, oxime(463358-39-6)
    11. EPA Substance Registry System: 4H-1-Benzopyran-4-one, 6-bromo-2-(4-methoxyphenyl)-, oxime(463358-39-6)

  • 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: 463358-39-6(Hazardous Substances Data)

463358-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 463358-39-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,6,3,3,5 and 8 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 463358-39:
(8*4)+(7*6)+(6*3)+(5*3)+(4*5)+(3*8)+(2*3)+(1*9)=166
166 % 10 = 6
So 463358-39-6 is a valid CAS Registry Number.

463358-39-6Downstream Products

463358-39-6Relevant articles and documents

Amino acid derivatives and oximes of flavones

Ishchenko,Shulyak,Khilya

, p. 274 - 280 (2002)

4-Ethoxyflavylium tetrafluoroborates with substituents in rings A and B were synthesized. Their reaction with nitrogen-containing nucleophiles was investigated. It was shown that derivatives of flavones at the carbonyl group are formed as a result of thes

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