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1000205-60-6

C32H28N2O4S2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1000205-60-6 Structure

  • Basic information

    1. Product Name: C32H28N2O4S2
    2. Synonyms: C32H28N2O4S2
    3. CAS NO:1000205-60-6
    4. Molecular Formula:
    5. Molecular Weight: 568.717
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1000205-60-6.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: C32H28N2O4S2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C32H28N2O4S2(1000205-60-6)
    11. EPA Substance Registry System: C32H28N2O4S2(1000205-60-6)

  • 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: 1000205-60-6(Hazardous Substances Data)

1000205-60-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1000205-60-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,0,2,0 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1000205-60:
(9*1)+(8*0)+(7*0)+(6*0)+(5*2)+(4*0)+(3*5)+(2*6)+(1*0)=46
46 % 10 = 6
So 1000205-60-6 is a valid CAS Registry Number.

1000205-60-6Upstream product

1000205-60-6Downstream Products

1000205-60-6Relevant articles and documents

Advancing palladium-catalyzed C-N bond formation: Bisindoline construction from successive amide transfer to internal alkenes

Muniz, Kilian

, p. 14542 - 14543 (2007)

The sequential transfer of two sulfonamides to internal alkenes affords the construction of vicinal diamines. In the presence of a palladium catalyst, the reaction proceeds through two mechanistically different C-N bond formation reactions. It is initiate

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