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896741-11-0

C7H8O3S*C10H19N3O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 896741-11-0 Structure

  • Basic information

    1. Product Name: C7H8O3S*C10H19N3O2
    2. Synonyms:
    3. CAS NO:896741-11-0
    4. Molecular Formula:
    5. Molecular Weight: 385.484
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 896741-11-0.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: C7H8O3S*C10H19N3O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C7H8O3S*C10H19N3O2(896741-11-0)
    11. EPA Substance Registry System: C7H8O3S*C10H19N3O2(896741-11-0)

  • 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: 896741-11-0(Hazardous Substances Data)

896741-11-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 896741-11-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,6,7,4 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 896741-11:
(8*8)+(7*9)+(6*6)+(5*7)+(4*4)+(3*1)+(2*1)+(1*1)=220
220 % 10 = 0
So 896741-11-0 is a valid CAS Registry Number.

896741-11-0Downstream Products

896741-11-0Relevant articles and documents

Keto-1,3,4-oxadiazoles as cathepsin K inhibitors

Palmer, James T.,Hirschbein, Bernard L.,Cheung, Harry,McCarter, John,Janc, James W.,Yu, Z. Walter,Wesolowski, Gregg

, p. 2909 - 2914 (2006)

We have prepared a series of cathepsin K inhibitors bearing the keto-1,3,4-oxadiazole warhead capable of forming a hemithioketal complex with the target enzyme. By modifying binding moieties at the P1, P2, and prime side positions of the inhibitors, we have achieved selectivity over cathepsins B, L, and S, and have achieved sub-nanomolar potency against cathepsin K. This series thus represents a promising chemotype that could be used in diseases implicated by imbalances in cathepsin K activity such as osteoporosis.

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