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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)-

4-Pyridinecarbonitrile, 2-hydroxy-

N#Cc1ccnc(c1)O Request for Quotation
Chemical Name: 4-Pyridinecarbonitrile, 2-hydroxy-
CAS Number: 95891-29-5
Product Number: AG01DDBM(AGN-PC-0OO8OK)
Synonyms:
MDL No: MFCD04037920
Molecular Formula: C6H4N2O
Molecular Weight: 120.10876

Identification/Properties

Computed Properties
Molecular Weight:
120.111g/mol
XLogP3:
-0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
120.032g/mol
Monoisotopic Mass:
120.032g/mol
Topological Polar Surface Area:
52.9A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
241
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Hydroxyisonicotinonitrile is a versatile compound that finds its application in various chemical synthesis processes. This compound serves as a key building block in the creation of pharmaceuticals, agrochemicals, and functional materials due to its unique chemical properties. In organic synthesis, 2-Hydroxyisonicotinonitrile can be used as a precursor for the synthesis of heterocyclic compounds, which are important in drug discovery and development. Its reactive nature allows for the introduction of different functional groups, making it a valuable intermediate in diverse synthetic pathways. Additionally, 2-Hydroxyisonicotinonitrile can participate in metal-catalyzed reactions, enabling the formation of complex molecular structures. Whether in the pharmaceutical industry for drug synthesis or in material science for the development of innovative materials, this compound plays a crucial role in advancing the field of chemical synthesis.