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76469-57-3

3-phenoxy-5-hydroxy-6-oxo-6H-anthra<1,9-cd>isoxazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 76469-57-3 Structure

  • Basic information

    1. Product Name: 3-phenoxy-5-hydroxy-6-oxo-6H-anthra<1,9-cd>isoxazole
    2. Synonyms: 3-phenoxy-5-hydroxy-6-oxo-6H-anthra<1,9-cd>isoxazole
    3. CAS NO:76469-57-3
    4. Molecular Formula:
    5. Molecular Weight: 329.312
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 76469-57-3.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-phenoxy-5-hydroxy-6-oxo-6H-anthra<1,9-cd>isoxazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-phenoxy-5-hydroxy-6-oxo-6H-anthra<1,9-cd>isoxazole(76469-57-3)
    11. EPA Substance Registry System: 3-phenoxy-5-hydroxy-6-oxo-6H-anthra<1,9-cd>isoxazole(76469-57-3)

  • 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: 76469-57-3(Hazardous Substances Data)

76469-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 76469-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,6 and 9 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 76469-57:
(7*7)+(6*6)+(5*4)+(4*6)+(3*9)+(2*5)+(1*7)=173
173 % 10 = 3
So 76469-57-3 is a valid CAS Registry Number.

76469-57-3Relevant articles and documents

TRANSFORMATIONS OF 1-AZIDO-2-ARYLOXYANTHRAQUINONES AND 3-ARYLOXYANTHRAISOXAZOL-6-ONES

Gornostaev, L. M.,Levdanskii, V. A.

, p. 1884 - 1890 (2007/10/02)

When heated, 1-azido-2-aryloxyanthraquinones undergo cyclization to 3-aryloxyanthraisoxazol-6-ones.As a result of thermolysis the latter are converted into 5,6-phthalylphenoxazines.The 5,6-phthalylphenoxazines are also obtained directly from 1-azido-2-aryloxyanthraquinones.Kinetic measurements showed that the conversion of the azides into 5,6-phthalylphenoxazines is a consecutive process involving the intermediate formation of 3-aryloxyanthraisoxazol-6-ones.

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