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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)-

1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-ol

COc1ccc(cc1)Cn1ncc2c1nccc2O Request for Quotation
Chemical Name: 1-(4-methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-ol
CAS Number: 924909-16-0
Product Number: AG019EV9(AG019EV9)
Synonyms:
MDL No:
Molecular Formula: C14H13N3O2
Molecular Weight: 255.2719

Identification/Properties

Computed Properties
Molecular Weight:
255.277g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
255.101g/mol
Monoisotopic Mass:
255.101g/mol
Topological Polar Surface Area:
56.2A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
364
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
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


1-(4-Methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-ol, also known as $name$, serves as a versatile building block in chemical synthesis processes. This compound plays a crucial role in the creation of novel pharmaceuticals, agrochemicals, and materials due to its unique structural properties and reactivity.In chemical synthesis, this compound can be utilized as a key intermediate in the production of various bioactive molecules and functional materials. Its heterocyclic structure provides opportunities for diversification through functional group manipulation, enabling the generation of a wide range of derivatives with tailored properties.Furthermore, the presence of the methoxybenzyl group offers a handle for selective chemical modifications, making it a valuable precursor in the construction of complex molecular architectures. The pyrazolo[3,4-b]pyridine core of this compound imparts specific structural motifs that are valuable in drug discovery and material science endeavors.Overall, the application of 1-(4-Methoxybenzyl)-1H-pyrazolo[3,4-b]pyridin-4-ol in chemical synthesis is instrumental in accessing structurally diverse compounds with potential applications in various industries.