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CAS

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473935-65-8

C13H12Cl6N2O7S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 473935-65-8 Structure

  • Basic information

    1. Product Name: C13H12Cl6N2O7S
    2. Synonyms: C13H12Cl6N2O7S
    3. CAS NO:473935-65-8
    4. Molecular Formula:
    5. Molecular Weight: 553.031
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 473935-65-8.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: C13H12Cl6N2O7S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C13H12Cl6N2O7S(473935-65-8)
    11. EPA Substance Registry System: C13H12Cl6N2O7S(473935-65-8)

  • 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: 473935-65-8(Hazardous Substances Data)

473935-65-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 473935-65-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,3,9,3 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 473935-65:
(8*4)+(7*7)+(6*3)+(5*9)+(4*3)+(3*5)+(2*6)+(1*5)=188
188 % 10 = 8
So 473935-65-8 is a valid CAS Registry Number.

473935-65-8Downstream Products

473935-65-8Relevant articles and documents

A mild, efficient method for the synthesis of aromatic and aliphatic sulfonamides

Chan, Wing Yan,Berthelette, Carl

, p. 4537 - 4540 (2002)

A two-step method was developed for the synthesis of aromatic and aliphatic sulfonamides from the corresponding sulfinates using bis(2,2,2-trichloroethyl)azodicarboxylate as the electrophilic nitrogen source. The intermediate sulfonylhydrazides were obtained in very good yields and were cleaved under reductive conditions to deliver the desired sulfonamides. A variety of substituents in the aromatic ring are well tolerated as well as heterocycles.

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