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1268396-48-0

C24H23NO10S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1268396-48-0 Structure

  • Basic information

    1. Product Name: C24H23NO10S
    2. Synonyms: C24H23NO10S
    3. CAS NO:1268396-48-0
    4. Molecular Formula:
    5. Molecular Weight: 517.513
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1268396-48-0.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: C24H23NO10S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C24H23NO10S(1268396-48-0)
    11. EPA Substance Registry System: C24H23NO10S(1268396-48-0)

  • 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: 1268396-48-0(Hazardous Substances Data)

1268396-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1268396-48-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,8,3,9 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1268396-48:
(9*1)+(8*2)+(7*6)+(6*8)+(5*3)+(4*9)+(3*6)+(2*4)+(1*8)=200
200 % 10 = 0
So 1268396-48-0 is a valid CAS Registry Number.

1268396-48-0Upstream product

1268396-48-0Relevant articles and documents

Lewis-acid-mediated domino reactions of Bis(diacetoxymethyl)-substituted arenes and heteroarenes

Clement, J. Arul,Sivasakthikumaran, Ramakrishnan,Mohanakrishnan, Arasambattu K.,Sundaramoorthy,Velmurugan, Devadasan

, p. 569 - 577 (2011)

A one-pot synthesis of annulated heterocycles involving a Lewis-acid-mediated domino reaction of bis(diacetoxymethyl)-substituted arenes and heteroarenes is described. The reaction of the tetraacetates with arenes and heteroarenes leads to the formation o

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