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1428522-15-9

C29H20N2O9 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1428522-15-9 Structure

  • Basic information

    1. Product Name: C29H20N2O9
    2. Synonyms: C29H20N2O9
    3. CAS NO:1428522-15-9
    4. Molecular Formula:
    5. Molecular Weight: 540.486
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1428522-15-9.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: C29H20N2O9(CAS DataBase Reference)
    10. NIST Chemistry Reference: C29H20N2O9(1428522-15-9)
    11. EPA Substance Registry System: C29H20N2O9(1428522-15-9)

  • 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: 1428522-15-9(Hazardous Substances Data)

1428522-15-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1428522-15-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,8,5,2 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1428522-15:
(9*1)+(8*4)+(7*2)+(6*8)+(5*5)+(4*2)+(3*2)+(2*1)+(1*5)=149
149 % 10 = 9
So 1428522-15-9 is a valid CAS Registry Number.

1428522-15-9Downstream Products

1428522-15-9Relevant articles and documents

Unexpected O-alkylation and ester migration in phenolic 2,3-diaryl-2,3-dihydrobenzo[b]furans

Tran, Henry,Dickson, Benjamin D.,Barker, David

, p. 2093 - 2096 (2013/04/23)

O-alkylation of 2-(4-methoxyphenyl)-5-hydroxy-3-[1,3-phenylene-bis(4- nitrobenzoate)]-2,3-dihydrobenzo[b]furan results in the unexpected hydrolysis of the nitrobenzoate esters, transfer of a 4-nitrobenzoic acid group to the 5-hydroxyl group and double alkylation of the newly formed 3,5-diphenol moiety. A range of alkyl halides can be used and give access to O-alkyl analogues of -viniferin.

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