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  • 1036243-37-4 Structure
  • Basic information

    1. Product Name: C22H19N3O3
    2. Synonyms: C22H19N3O3
    3. CAS NO:1036243-37-4
    4. Molecular Formula:
    5. Molecular Weight: 373.411
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1036243-37-4.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: C22H19N3O3(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H19N3O3(1036243-37-4)
    11. EPA Substance Registry System: C22H19N3O3(1036243-37-4)
  • 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: 1036243-37-4(Hazardous Substances Data)

1036243-37-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1036243-37-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,6,2,4 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1036243-37:
(9*1)+(8*0)+(7*3)+(6*6)+(5*2)+(4*4)+(3*3)+(2*3)+(1*7)=114
114 % 10 = 4
So 1036243-37-4 is a valid CAS Registry Number.

1036243-37-4Upstream product

1036243-37-4Downstream Products

1036243-37-4Relevant articles and documents

Janus kinase 2 inhibitors. Synthesis and characterization of a novel polycyclic azaindole

, p. 7938 - 7941 (2009)

The synthesis and characterization of a novel polycyclic azaindole based derivative is disclosed, and its binding to JAK2 is described. The compound is further evaluated for its ability to block the EPO/JAK2 signaling cascade in vitro and in vivo.

TRICYCLIC HETEROARYL COMPOUNDS USEFUL AS INHIBITORS OF JANUS KINASE

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Page/Page column 35, (2010/04/25)

The present invention relates to compounds useful as inhibitors of protein kinases, particularly of JAK family kinases. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compositions in

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