2-chloro-3-methylpyrazolo[1,5-a]pyridine|1428432-88-5,AngeneChemical

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Pyrimidine, 5-bromo-2-methyl-

1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide

2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-

O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]

Tris(dibenzylideneacetone)dipalladium

C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C

Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

2-chloro-3-methylpyrazolo[1,5-a]pyridine

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Chemical Name:	2-chloro-3-methylpyrazolo[1,5-a]pyridine
CAS Number:	1428432-88-5
Product Number:	AG00HWPB(AGN-PC-0JK1SB)
Synonyms:
MDL No:
Molecular Formula:	C8H7ClN2
Molecular Weight:	166.60758

Identification/Properties
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Identification/Properties

Safety Information

GHS Pictogram:

Signal Word:

Warning

UN#:

N/A

Hazard Statements:

H302-H315-H319-H335

Precautionary Statements:

P261-P305+P351+P338

Class:

N/A

Packing Group:

N/A

NMR Spectrum

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Chemical Structure

2-Chloro-3-methylpyrazolo[1,5-a]pyridine serves as a versatile building block in chemical synthesis due to its unique molecular structure and reactivity. This compound can be utilized in the preparation of various heterocyclic compounds through cyclization reactions. Its halogen substituent allows for further functionalization, enabling the introduction of specific chemical groups at the chloro position. Additionally, the presence of the pyridine and pyrazole rings in its structure imparts diverse properties that make it a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its application extends to the development of novel materials and bioactive molecules, highlighting its significance in modern organic chemistry.