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1011726-37-6

C34H29F5N2O4S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1011726-37-6 Structure

  • Basic information

    1. Product Name: C34H29F5N2O4S
    2. Synonyms:
    3. CAS NO:1011726-37-6
    4. Molecular Formula:
    5. Molecular Weight: 656.673
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1011726-37-6.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: C34H29F5N2O4S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C34H29F5N2O4S(1011726-37-6)
    11. EPA Substance Registry System: C34H29F5N2O4S(1011726-37-6)

  • 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: 1011726-37-6(Hazardous Substances Data)

1011726-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1011726-37-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,1,7,2 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1011726-37:
(9*1)+(8*0)+(7*1)+(6*1)+(5*7)+(4*2)+(3*6)+(2*3)+(1*7)=96
96 % 10 = 6
So 1011726-37-6 is a valid CAS Registry Number.

1011726-37-6Upstream product

1011726-37-6Downstream Products

1011726-37-6Relevant articles and documents

Potency and selectivity of P2/P3-modified inhibitors of cysteine proteases from trypanosomes

Jaishankar, Priyadarshini,Hansell, Elizabeth,Zhao, Dong-Mei,Doyle, Patricia S.,McKerrow, James H.,Renslo, Adam R.

, p. 624 - 628 (2008)

A systematic study of P2 and P3 substitution in a series of vinyl sulfone cysteine protease inhibitors is described. The introduction of a methyl substituent in the P2 phenylalanine aryl ring had a favorable effect on protease inhibition and conferred modest selectivity for rhodesain over cruzain. Rhodesain selectivity could be enhanced further by combining these P2 modifications with certain P3 amide substituents.

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