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957060-05-8

C38H40N2O4S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 957060-05-8 Structure

  • Basic information

    1. Product Name: C38H40N2O4S
    2. Synonyms:
    3. CAS NO:957060-05-8
    4. Molecular Formula:
    5. Molecular Weight: 620.813
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 957060-05-8.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: C38H40N2O4S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C38H40N2O4S(957060-05-8)
    11. EPA Substance Registry System: C38H40N2O4S(957060-05-8)

  • 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: 957060-05-8(Hazardous Substances Data)

957060-05-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 957060-05-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,0,6 and 0 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 957060-05:
(8*9)+(7*5)+(6*7)+(5*0)+(4*6)+(3*0)+(2*0)+(1*5)=178
178 % 10 = 8
So 957060-05-8 is a valid CAS Registry Number.

957060-05-8Upstream product

957060-05-8Downstream Products

957060-05-8Relevant articles and documents

Discovery of potent HIV-1 protease inhibitors incorporating sulfoximine functionality

Lu, Ding,Vince, Robert

, p. 5614 - 5619 (2007)

Based on the unique property of sulfoximine and the homodimeric C2 structural symmetry of HIV-1 protease, a novel class of sulfoximine-based pseudosymmetric HIV-1 protease inhibitors was designed and synthesized. The sulfoximine moiety was demonstrated to be important for HIV-1 protease inhibitor potency. The most active stereoisomer (2S,2′S) displays a potency of 2.5 nM (IC50) against HIV-1 protease and an anti-HIV-1 activity of 408 nM (IC50). A possible mode of action is proposed.

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