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  • 1229611-83-9 Structure
  • Basic information

    1. Product Name: C33H23F4N5O3S
    2. Synonyms:
    3. CAS NO:1229611-83-9
    4. Molecular Formula:
    5. Molecular Weight: 645.637
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1229611-83-9.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: C33H23F4N5O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C33H23F4N5O3S(1229611-83-9)
    11. EPA Substance Registry System: C33H23F4N5O3S(1229611-83-9)
  • 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: 1229611-83-9(Hazardous Substances Data)

1229611-83-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1229611-83-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,9,6,1 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1229611-83:
(9*1)+(8*2)+(7*2)+(6*9)+(5*6)+(4*1)+(3*1)+(2*8)+(1*3)=149
149 % 10 = 9
So 1229611-83-9 is a valid CAS Registry Number.

1229611-83-9Downstream Products

1229611-83-9Relevant articles and documents

Identification of a novel series of potent RON receptor tyrosine kinase inhibitors

Raeppel, Stéphane,Gaudette, Frédéric,Mannion, Michael,Claridge, Stephen,Saavedra, Oscar,Isakovic, Ljubomir,Déziel, Robert,Beaulieu, Normand,Beaulieu, Carole,Dupont, Isabelle,Nguyen, Hannah,Wang, James,Macleod, A. Robert,Maroun, Christiane,Besterman, Jeffrey M.,Vaisburg, Arkadii

scheme or table, p. 2745 - 2749 (2010/07/15)

A novel series of N-(3-fluoro-4-(2-substituted-thieno[3,2-b]pyridin-7-yloxy)phenyl)-1-phenyl-5-(trifluoromethyl)-1H-pyrazole-4-carboxamides targeting RON receptor tyrosine kinase was designed and synthesized. SAR study of the series allowed us to identify compounds possessing either inhibitory activity of RON kinase enzyme in the low nanomolar range with low residual activity against the closely related c-Met or potent dual inhibitory activity against RON and c-Met, - with no significant activity against VEGFR2 in both cases.

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