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1197053-77-2

C24H34IN3O8S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1197053-77-2 Structure

  • Basic information

    1. Product Name: C24H34IN3O8S
    2. Synonyms: C24H34IN3O8S
    3. CAS NO:1197053-77-2
    4. Molecular Formula:
    5. Molecular Weight: 651.52
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1197053-77-2.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: C24H34IN3O8S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C24H34IN3O8S(1197053-77-2)
    11. EPA Substance Registry System: C24H34IN3O8S(1197053-77-2)

  • 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: 1197053-77-2(Hazardous Substances Data)

1197053-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1197053-77-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,7,0,5 and 3 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1197053-77:
(9*1)+(8*1)+(7*9)+(6*7)+(5*0)+(4*5)+(3*3)+(2*7)+(1*7)=172
172 % 10 = 2
So 1197053-77-2 is a valid CAS Registry Number.

1197053-77-2Downstream Products

1197053-77-2Relevant articles and documents

A convenient catalyst for aqueous and protein Suzuki-Miyaura cross-coupling

Chalker, Justin M.,Wood, Charlotte S. C.,Davis, Benjamin G.

supporting information; experimental part, p. 16346 - 16347 (2010/01/29)

(Figure Presented) A phosphine-free palladium catalyst for aqueous Suzuki-Miyaura cross-coupling is presented. The catalyst is active enough to mediate hindered, ortho-substituted biaryl couplings but mild enough for use on peptides and proteins. The Suzuki-Miyaura couplings on protein substrates are the first to proceed in useful conversions. Notably, hydrophobic aryl and vinyl groups can be transferred to the protein surface without the aid of organic solvent since the aryl- and vinylboronic acids used in the coupling are water-soluble as borate salts. The convenience and activity of this catalyst prompts use in both general synthesis and bioconjugation.

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