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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)-

3H-Pyrazolo[3,4-b]pyridin-3-one, 1,2-dihydro-

O=c1[nH][nH]c2c1cccn2 Request for Quotation
Chemical Name: 3H-Pyrazolo[3,4-b]pyridin-3-one, 1,2-dihydro-
CAS Number: 2942-43-0
Product Number: AG002YBM(AGN-PC-0JR0G9)
Synonyms:
MDL No:
Molecular Formula: C6H5N3O
Molecular Weight: 135.1234

Identification/Properties

Properties
MP:
234-236°
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
135.126g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
135.043g/mol
Monoisotopic Mass:
135.043g/mol
Topological Polar Surface Area:
54A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
159
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


1H-Pyrazolo[3,4-b]pyridin-3(2H)-one, also known by its chemical structure, is a versatile compound widely utilized in chemical synthesis as a key intermediate for the development of various pharmaceuticals, agrochemicals, and materials. This heterocyclic scaffold serves as a valuable building block in the synthesis of organic compounds due to its unique structural properties and functional groups. In chemical synthesis, 1H-Pyrazolo[3,4-b]pyridin-3(2H)-one acts as a precursor for the preparation of diverse derivatives with enhanced biological activities and desirable physical properties. Its inclusion in synthetic pathways allows for the introduction of specific functionalities and structural motifs that are crucial for the desired pharmacological or material properties. This compound can undergo various reactions such as acylation, alkylation, oxidation, and reduction, enabling the modification and optimization of its chemical properties for a wide range of applications.Furthermore, the incorporation of 1H-Pyrazolo[3,4-b]pyridin-3(2H)-one in chemical synthesis provides researchers and chemists with a valuable tool for the creation of novel compounds with potential applications in drug discovery, crop protection, and material science. Its versatility and reactivity make it a valuable component in the design and synthesis of complex molecules with tailored properties, making it a key player in modern organic chemistry research and development.