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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
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)-

Pyrazolo[1,5-a]pyridine-3-carboxylic acid, 5-methoxy-, ethyl ester

CCOC(=O)c1cnn2c1cc(OC)cc2 Request for Quotation
Chemical Name: Pyrazolo[1,5-a]pyridine-3-carboxylic acid, 5-methoxy-, ethyl ester
CAS Number: 99446-53-4
Product Number: AG00IKAA(AGN-PC-00MW6S)
Synonyms:
MDL No:
Molecular Formula: C11H12N2O3
Molecular Weight: 220.2246

Identification/Properties

Computed Properties
Molecular Weight:
220.228g/mol
XLogP3:
1.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
220.085g/mol
Monoisotopic Mass:
220.085g/mol
Topological Polar Surface Area:
52.8A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
260
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 5-methoxypyrazolo[1,5-a]pyridine-3-carboxylate is a versatile chemical compound commonly used in chemical synthesis as a key building block. Its unique chemical structure and reactivity make it an essential component in the production of various pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, Ethyl 5-methoxypyrazolo[1,5-a]pyridine-3-carboxylate serves as a valuable intermediate for the synthesis of pyrazole derivatives and heterocyclic compounds. Its presence in a reaction mixture can facilitate the formation of complex molecular structures through diverse chemical transformations, such as substitution, addition, and cyclization reactions.Moreover, this compound exhibits excellent compatibility with a wide range of reagents and catalysts, making it a preferred choice for organic chemists seeking to efficiently construct molecules with specific functionalities. Its strategic placement of functional groups enables precise control over regioselectivity and stereochemistry, enhancing the synthetic efficiency of complex molecule assembly.Beyond its role as a synthetic intermediate, Ethyl 5-methoxypyrazolo[1,5-a]pyridine-3-carboxylate also imparts unique pharmacological properties to the final products, making it an attractive candidate for drug discovery and development. Its presence in the molecular structure can influence the biological activity, pharmacokinetic profile, and metabolic stability of the target compounds, thereby enhancing their therapeutic potential.Overall, Ethyl 5-methoxypyrazolo[1,5-a]pyridine-3-carboxylate is a valuable tool in the hands of synthetic chemists, enabling the efficient synthesis of diverse molecular architectures with applications ranging from pharmaceuticals to agrochemicals. Its versatile reactivity and compatibility make it a valuable asset in modern chemical synthesis strategies for the creation of novel and complex molecules.