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ChemicalBook--->CAS DataBase List--->274-56-6

274-56-6

274-56-6 Structure

274-56-6 Structure
IdentificationBack Directory
[Name]

Pyrazolo[1,5-a]pyridine
[CAS]

274-56-6
[Synonyms]

3-Azaindoline
PYRAZOLO[1,5-A]PYRIDINE
1H-Pyrazolo[1,5-a]pyridine
Pyrazolo[1,5-a]pyridine,97%
6,7a-dimethyl-2,3,5,6-tetrahydrooxazolo[2,3-b]oxazole
[Molecular Formula]

C7H6N2
[MDL Number]

MFCD08752622
[MOL File]

274-56-6.mol
[Molecular Weight]

118.14
Chemical PropertiesBack Directory
[Boiling point ]

37-39℃/0.2mm
[density ]

1.14±0.1 g/cm3(Predicted)
[refractive index ]

1.6075
[storage temp. ]

Sealed in dry,Room Temperature
[form ]

Liquid
[pka]

2.83±0.30(Predicted)
[color ]

Colorless to red or brown
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P261-P280a-P304+P340-P305+P351+P338-P405-P501a
[HS Code ]

2933399990
Hazard InformationBack Directory
[Description]

Pyrazolo[1,5-a]pyridines, a class of fused heteroaromatic bicyclic compounds, have been investigated for their pharmacological and biological activities. They are used as dopamine D2/D3/D4 antagonists, anti-herpetic agents, p38 kinase inhibitors, PI3 kinase inhibitors, antitubercular agents, EP1 receptor antagonists, 5HT3-antagonists, melatonin receptor (MT1/MT2) ligands, Mcl-1Bcl-xL dual inhibitors, and corticotropin-releasing factor 1 antagonists. Pyrazolo[1,5-a]pyridine has been used as a fluorophore in the research of Zhang et al. and exhibited high quantum yield (0.64, pH 2.4), high selectivity and sensitivity, and extremely short response time[1].
[References]

[1] Brian A Johns. “Pyrazolo[1,5-a]pyridines: synthetic approaches to a novel class of antiherpetics.” Tetrahedron 59 45 (2003): Pages 9001-9011.
Spectrum DetailBack Directory
[Spectrum Detail]

Pyrazolo[1,5-a]pyridine(274-56-6)1HNMR
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