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207279-29-6

8-Methoxy-1,7-naphthyridin-6-yl trifluoroMethanesulfonate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 207279-29-6 Structure

  • Basic information

    1. Product Name: 8-Methoxy-1,7-naphthyridin-6-yl trifluoroMethanesulfonate
    2. Synonyms: 8-Methoxy-1,7-naphthyridin-6-yl trifluoroMethanesulfonate
    3. CAS NO:207279-29-6
    4. Molecular Formula: C10H7F3N2O4S
    5. Molecular Weight: 308.2337896
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 207279-29-6.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 8-Methoxy-1,7-naphthyridin-6-yl trifluoroMethanesulfonate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-Methoxy-1,7-naphthyridin-6-yl trifluoroMethanesulfonate(207279-29-6)
    11. EPA Substance Registry System: 8-Methoxy-1,7-naphthyridin-6-yl trifluoroMethanesulfonate(207279-29-6)

  • 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: 207279-29-6(Hazardous Substances Data)

207279-29-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 207279-29-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,7,2,7 and 9 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 207279-29:
(8*2)+(7*0)+(6*7)+(5*2)+(4*7)+(3*9)+(2*2)+(1*9)=136
136 % 10 = 6
So 207279-29-6 is a valid CAS Registry Number.

207279-29-6Relevant articles and documents

Synthesis of 4-(8-benzo[1,2,5]oxadiazol-5-yl-[1,7]naphthyridine-6-yl)-benzoic acid: A potent and selective phosphodiesterase type 4D inhibitor

Hersperger, Rene,Dawson, Janet,Mueller, Thomas

, p. 233 - 235 (2002)

The synthesis of a 6,8-disubstituted 1,7-naphthyridine 1 and its characterization as a potent and selective phosphodiesterase type 4D inhibitor (IC50=1.5nM) are described. The compound inhibited TNFα-release from human peripheral blood mononuclear cells and was orally active in a model of adjuvant-induced arthritis in rats.

INHIBITORS OF PI3 KINASE

-

Page/Page column 129, (2010/01/12)

The present invention relates to compounds of Formula (I), or a pharmaceutically acceptable salt thereof; methods of treating diseases or conditions, such as cancer, using the compounds; and pharmaceutical compositions containing the compounds, wherein Q, X1, X2, R1 and Z are as defined herein.

Naphthyridine derivatives

-

, (2008/06/13)

PCT No. PCT/EP97/05898 Sec. 371 Date Apr. 27, 1999 Sec. 102(e) Date Apr. 27, 1999 PCT Filed Oct. 24, 1997 PCT Pub. No. WO98/18796 PCT Pub. Date May 7, 1998Novel 8-aryl-1,7-naphthyridines, in free or salt form, are PDE IV inhibitors and are thus useful as pharmaceuticals, e.g. for asthma therapy. Preferred compounds include compounds of formulae (I and II) wherein the R groups are as defined. Pharmaceutical compositions comprising the compounds, processes for preparation of the compounds and novel intermediates for use in the processes are disclosed.

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