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780752-59-2

C21H25ClN6O2 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 780752-59-2 Structure

  • Basic information

    1. Product Name: C21H25ClN6O2
    2. Synonyms:
    3. CAS NO:780752-59-2
    4. Molecular Formula:
    5. Molecular Weight: 428.922
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 780752-59-2.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: C21H25ClN6O2(CAS DataBase Reference)
    10. NIST Chemistry Reference: C21H25ClN6O2(780752-59-2)
    11. EPA Substance Registry System: C21H25ClN6O2(780752-59-2)

  • 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: 780752-59-2(Hazardous Substances Data)

780752-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 780752-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,0,7,5 and 2 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 780752-59:
(8*7)+(7*8)+(6*0)+(5*7)+(4*5)+(3*2)+(2*5)+(1*9)=192
192 % 10 = 2
So 780752-59-2 is a valid CAS Registry Number.

780752-59-2Downstream Products

780752-59-2Relevant articles and documents

Design and synthesis of bicyclic pyrazinone and pyrimidinone amides as potent TF-FVIIa inhibitors

Zhang, Xiaojun,Glunz, Peter W.,Jiang, Wen,Schmitt, Aaron,Newman, Makenzie,Barbera, Frank A.,Bozarth, Jeffery M.,Rendina, Alan R.,Wei, Anzhi,Wen, Xiao,Rossi, Karen A.,Luettgen, Joseph M.,Wong, Pancras C.,Knabb, Robert M.,Wexler, Ruth R.,Scott Priestley

, p. 1604 - 1607 (2013/04/10)

Bicyclic pyrazinone and pyrimidinone amides were designed and synthesized as potent TF-FVIIa inhibitors. SAR demonstrated that the S2 and S3 pockets of FVIIa prefer to bind small, lipophilic groups. An X-ray crystal structure of optimized compound 9b boun

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