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1021298-36-1

C40H36N2O12 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1021298-36-1 Structure

  • Basic information

    1. Product Name: C40H36N2O12
    2. Synonyms: C40H36N2O12
    3. CAS NO:1021298-36-1
    4. Molecular Formula:
    5. Molecular Weight: 736.732
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1021298-36-1.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: C40H36N2O12(CAS DataBase Reference)
    10. NIST Chemistry Reference: C40H36N2O12(1021298-36-1)
    11. EPA Substance Registry System: C40H36N2O12(1021298-36-1)

  • 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: 1021298-36-1(Hazardous Substances Data)

1021298-36-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1021298-36-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,1,2,9 and 8 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1021298-36:
(9*1)+(8*0)+(7*2)+(6*1)+(5*2)+(4*9)+(3*8)+(2*3)+(1*6)=111
111 % 10 = 1
So 1021298-36-1 is a valid CAS Registry Number.

1021298-36-1Upstream product

1021298-36-1Downstream Products

1021298-36-1Relevant articles and documents

Asymmetric biomimetic oxidations of phenols: The mechanism of the diastereo- and enantioselective synthesis of thomasidioic acid

Zoia, Luca,Bruschi, Maurizio,Orlandi, Marco,Tolppa, Eeva-Liisa,Rindone, Bruno

, p. 129 - 148 (2008/09/17)

Enantiopure chiral amidic derivatives of sinapic acid were oxidised with hydrogen peroxide using horseradish peroxidase (HRP) as the catalyst to give the aryltetraline dilignol thomasidioic acid. Trans-diastereoselectivity and enantioselectivity in the fo

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