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291744-01-9

6-CHLORO-2-(4-FLUOROPHENYL)PYRAZOLO[1,5-A]PYRIDINE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 291744-01-9 Structure

  • Basic information

    1. Product Name: 6-CHLORO-2-(4-FLUOROPHENYL)PYRAZOLO[1,5-A]PYRIDINE
    2. Synonyms: 6-CHLORO-2-(4-FLUOROPHENYL)PYRAZOLO[1,5-A]PYRIDINE
    3. CAS NO:291744-01-9
    4. Molecular Formula: C13H8ClFN2
    5. Molecular Weight: 246.67
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 291744-01-9.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: 6-CHLORO-2-(4-FLUOROPHENYL)PYRAZOLO[1,5-A]PYRIDINE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-CHLORO-2-(4-FLUOROPHENYL)PYRAZOLO[1,5-A]PYRIDINE(291744-01-9)
    11. EPA Substance Registry System: 6-CHLORO-2-(4-FLUOROPHENYL)PYRAZOLO[1,5-A]PYRIDINE(291744-01-9)

  • 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: 291744-01-9(Hazardous Substances Data)

291744-01-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 291744-01-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,1,7,4 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 291744-01:
(8*2)+(7*9)+(6*1)+(5*7)+(4*4)+(3*4)+(2*0)+(1*1)=149
149 % 10 = 9
So 291744-01-9 is a valid CAS Registry Number.

291744-01-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-CHLORO-2-(4-FLUOROPHENYL)PYRAZOLO[1,5-A]PYRIDINE

1.2 Other means of identification

Product number -
Other names 2-(4-Fluorophenyl)-6-chloropyrazolo[1,5-a]pyridine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:291744-01-9 SDS

291744-01-9Downstream Products

291744-01-9Relevant articles and documents

Synthesis of 2-Arylpyrazolo[1,5- a ]pyridines by Suzuki-Miyaura Cross-Coupling Reaction

Umei, Kentaro,Nishigaya, Yosuke,Kamiya, Megumi,Kohno, Yasushi,Seto, Shigeki

, p. 3221 - 3230 (2015/10/19)

Convenient access to a variety of 2-arylated pyrazolo[1,5-a]pyridine via pyrazolo[1,5-a]pyridine-2-yl triflate using the Suzuki-MiyauraA AA cross-coupling reaction is described. Fifteen 2-arylpyrazolo[1,5-a]pyridine derivatives were synthesized in 52-95% yields.

The identification of pyrazolo[1,5-a]pyridines as potent p38 kinase inhibitors

Cheung, Mui,Harris, Philip A.,Badiang, Jennifer G.,Peckham, Gregory E.,Chamberlain, Stanley D.,Alberti, Michael J.,Jung, David K.,Harris, Stephanie S.,Bramson, Neal H.,Epperly, Andrea H.,Stimpson, Stephen A.,Peel, Michael R.

scheme or table, p. 5428 - 5430 (2009/06/18)

A series of pyrazolo[1,5-a]pyridine derivatives was designed and synthesized as novel potent p38 kinase inhibitors. Our approaches towards improving in vitro metabolism and in vivo pharmacokinetic properties of the series are described.

Fused pyrazole derivatives bieng protein kinase inhibitors

-

, (2008/06/13)

Compounds of Formula (I): salts or solvates or physiologically functional derivatives thereof, wherein Z is CH or N, and R1, (R2, and R4 are various substituent groups, are protein kinase inhibitors.

Pyrazolopyridines

-

, (2008/06/13)

The invention provides the compounds of formula (I) wherein: R0and R1are independently selected from H, halogen, C1-6alkyl, C1-6alkoxy, or C1-6alkoxy substituted by one or more fluorine atoms; R2

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