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CAS

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1356832-80-8

C20H17(2)H2NO7S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1356832-80-8 Structure

  • Basic information

    1. Product Name: C20H17(2)H2NO7S
    2. Synonyms: C20H17(2)H2NO7S
    3. CAS NO:1356832-80-8
    4. Molecular Formula:
    5. Molecular Weight: 419.423
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1356832-80-8.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: C20H17(2)H2NO7S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C20H17(2)H2NO7S(1356832-80-8)
    11. EPA Substance Registry System: C20H17(2)H2NO7S(1356832-80-8)

  • 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: 1356832-80-8(Hazardous Substances Data)

1356832-80-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1356832-80-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,6,8,3 and 2 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1356832-80:
(9*1)+(8*3)+(7*5)+(6*6)+(5*8)+(4*3)+(3*2)+(2*8)+(1*0)=178
178 % 10 = 8
So 1356832-80-8 is a valid CAS Registry Number.

1356832-80-8Downstream Products

1356832-80-8Relevant articles and documents

Rhodium catalyzed C-H olefination of N-benzoylsulfonamides with internal alkenes

Zhu, Chen,Falck, John R.

supporting information; experimental part, p. 1674 - 1676 (2012/03/11)

An annulation via tandem rhodium catalyzed C-H olefination of N-benzoylsulfonamides with internal olefins followed by C-N bond formation is disclosed. A N-substituted quaternary center is formed during the reaction thus providing efficient access to a series of 3,3-disubstituted isoindolinones. The Royal Society of Chemistry 2012.

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