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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 1H-pyrazolo[4,3-b]pyridine-3-carboxylate

COC(=O)c1n[nH]c2c1nccc2 Request for Quotation
Chemical Name: methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate
CAS Number: 1260891-66-4
Product Number: AG000RJV(AGN-PC-0JF3RU)
Synonyms:
MDL No:
Molecular Formula: C8H7N3O2
Molecular Weight: 177.1601

Identification/Properties

Computed Properties
Molecular Weight:
177.163g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
177.054g/mol
Monoisotopic Mass:
177.054g/mol
Topological Polar Surface Area:
67.9A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
210
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 1H-pyrazolo[4,3-b]pyridine-3-carboxylate is a versatile compound widely utilized in chemical synthesis for the development of various pharmaceuticals and agrochemicals. As a key intermediate in organic synthesis, this compound serves as a building block in the creation of complex molecules with significant biological activities. Its unique structural properties make it especially valuable in the modification and design of novel compounds for drug discovery and development purposes. In chemical synthesis, Methyl 1H-pyrazolo[4,3-b]pyridine-3-carboxylate plays a crucial role in the construction of heterocyclic frameworks and the introduction of specific functional groups, contributing to the synthesis of diverse compounds with potential applications in the fields of medicine and agriculture.