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1344028-49-4

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

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  • 1344028-49-4 Structure

  • Basic information

    1. Product Name: 2',4',5,7-tetramethoxymethoxyisoflavone
    2. Synonyms: 2',4',5,7-tetramethoxymethoxyisoflavone
    3. CAS NO:1344028-49-4
    4. Molecular Formula:
    5. Molecular Weight: 462.453
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1344028-49-4.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: 2',4',5,7-tetramethoxymethoxyisoflavone(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2',4',5,7-tetramethoxymethoxyisoflavone(1344028-49-4)
    11. EPA Substance Registry System: 2',4',5,7-tetramethoxymethoxyisoflavone(1344028-49-4)

  • 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: 1344028-49-4(Hazardous Substances Data)

1344028-49-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1344028-49-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,4,0,2 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1344028-49:
(9*1)+(8*3)+(7*4)+(6*4)+(5*0)+(4*2)+(3*8)+(2*4)+(1*9)=134
134 % 10 = 4
So 1344028-49-4 is a valid CAS Registry Number.

1344028-49-4Relevant articles and documents

Total synthesis of the pyranocoumaronochromone lupinalbin H

Selepe, Mamoalosi A.,Drewes, Siegfried E.,Van Heerden, Fanie R.

, p. 8654 - 8658 (2011/12/01)

The pyranocoumaronochromone lupinalbin H was synthesized in three major steps, which involved preparation of 2′-hydroxygenistein by the Suzuki-Miyaura reaction, followed by oxidative cyclodehydrogenation into lupinalbin A. The final step was the regiospec

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