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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)-

Methyl 5-formylpyrazolo[1,5-a]pyridine-3-carboxylate

COC(=O)c1cnn2c1cc(C=O)cc2 Request for Quotation
Chemical Name: Methyl 5-formylpyrazolo[1,5-a]pyridine-3-carboxylate
CAS Number: 936637-97-7
Product Number: AG00H5KB(AGN-PC-0WAMDJ)
Synonyms:
MDL No: MFCD16987698
Molecular Formula: C10H8N2O3
Molecular Weight: 204.1821

Identification/Properties

Computed Properties
Molecular Weight:
204.185g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
204.053g/mol
Monoisotopic Mass:
204.053g/mol
Topological Polar Surface Area:
60.7A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
269
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:
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

Other Analytical Data

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Chemical Structure


Methyl 5-formylpyrazolo[1,5-a]pyridine-3-carboxylate is a versatile compound widely utilized in chemical synthesis as a key building block. Its unique structure and reactivity make it a valuable tool in various synthetic pathways. In organic chemistry, this compound serves as a precursor for the synthesis of diverse heterocyclic compounds with pharmaceutical and agrochemical significance. Additionally, its presence in the synthetic toolkit enables the construction of complex molecules through multi-step synthetic routes. The strategic incorporation of Methyl 5-formylpyrazolo[1,5-a]pyridine-3-carboxylate in synthetic schemes facilitates the generation of novel compounds with tailored properties for various applications in the field of chemistry.