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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]pyridin-5-ylmethanol

OCc1ccn2c(c1)ccn2 Request for Quotation
Chemical Name: pyrazolo[1,5-a]pyridin-5-ylmethanol
CAS Number: 474432-57-0
Product Number: AG00DBGC(AGN-PC-0NFFZJ)
Synonyms:
MDL No:
Molecular Formula: C8H8N2O
Molecular Weight: 148.16192

Identification/Properties

Computed Properties
Molecular Weight:
148.165g/mol
XLogP3:
0.2
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
148.064g/mol
Monoisotopic Mass:
148.064g/mol
Topological Polar Surface Area:
37.5A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
140
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


Pyrazolo[1,5-a]pyridin-5-ylmethanol is a versatile compound widely used in chemical synthesis due to its unique structure and reactivity. This molecule serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and materials.One prominent application of Pyrazolo[1,5-a]pyridin-5-ylmethanol is its role as a key intermediate in the synthesis of novel heterocyclic compounds. Its ability to undergo diverse chemical transformations, such as oxidation, reduction, and substitution reactions, allows for the creation of structurally complex molecules with specific desired properties.Furthermore, Pyrazolo[1,5-a]pyridin-5-ylmethanol is utilized in the development of bioactive molecules with potential pharmaceutical applications. By incorporating this compound into drug design, chemists can explore its interactions with biological targets and assess its therapeutic potential in treating various diseases.In summary, the significance of Pyrazolo[1,5-a]pyridin-5-ylmethanol in chemical synthesis lies in its versatility as a starting material for the construction of diverse compounds with potential industrial and pharmaceutical relevance.