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CAS

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256486-45-0

3,3',4',5,5',7-hexahydroxy-2',6,6',8-tetranitroflavone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 256486-45-0 Structure

  • Basic information

    1. Product Name: 3,3',4',5,5',7-hexahydroxy-2',6,6',8-tetranitroflavone
    2. Synonyms: 3,3',4',5,5',7-hexahydroxy-2',6,6',8-tetranitroflavone
    3. CAS NO:256486-45-0
    4. Molecular Formula:
    5. Molecular Weight: 498.23
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 256486-45-0.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: 3,3',4',5,5',7-hexahydroxy-2',6,6',8-tetranitroflavone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,3',4',5,5',7-hexahydroxy-2',6,6',8-tetranitroflavone(256486-45-0)
    11. EPA Substance Registry System: 3,3',4',5,5',7-hexahydroxy-2',6,6',8-tetranitroflavone(256486-45-0)

  • 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: 256486-45-0(Hazardous Substances Data)

256486-45-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 256486-45-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,4,8 and 6 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 256486-45:
(8*2)+(7*5)+(6*6)+(5*4)+(4*8)+(3*6)+(2*4)+(1*5)=170
170 % 10 = 0
So 256486-45-0 is a valid CAS Registry Number.

256486-45-0Upstream product

256486-45-0Downstream Products

256486-45-0Relevant articles and documents

Chemical modification of the natural flavonoid myricetin

Polyakov

, p. 21 - 28 (2007/10/03)

A review is presented of our own results on the synthesis of nitro-, amino-, azo-, and bromo-derivatives of myricetin, as a result which 19 new derivatives have been obtained. The compounds synthesized are of interest as substances with potential antitumo

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