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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]pyridine-3-carbonitrile

N#Cc1cnn2c1cccc2 Request for Quotation
Chemical Name: Pyrazolo[1,5-a]pyridine-3-carbonitrile
CAS Number: 25627-89-8
Product Number: AG00BHRE(AGN-PC-00JXE1)
Synonyms:
MDL No:
Molecular Formula: C8H5N3
Molecular Weight: 143.1454

Identification/Properties

Computed Properties
Molecular Weight:
143.15g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
143.048347g/mol
Monoisotopic Mass:
143.048347g/mol
Topological Polar Surface Area:
41.1Ų
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
193
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-P280-P301+P312-P302+P352-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]pyridine-3-carbonitrile is a versatile compound that plays a significant role in chemical synthesis. Its unique structure and reactivity make it a valuable building block in the creation of various organic molecules and pharmaceutical compounds. This compound can act as a key intermediate in the synthesis of complex heterocyclic compounds, offering a convenient pathway for the construction of diverse molecular structures. Its presence in a synthesis pathway can enable the introduction of functional groups or modifications that are essential for enhancing the biological activity or physical properties of the final product. Additionally, Pyrazolo[1,5-a]pyridine-3-carbonitrile's compatibility with a wide range of reaction conditions and its ability to participate in various chemical transformations make it a valuable tool for organic chemists seeking to design and develop novel compounds with tailored properties.