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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)-

2-Pyridinecarboxylic acid, 5-cyano-

N#Cc1ccc(nc1)C(=O)O Request for Quotation
Chemical Name: 2-Pyridinecarboxylic acid, 5-cyano-
CAS Number: 53234-55-2
Product Number: AG00DAGD(AGN-PC-0OBUCN)
Synonyms:
MDL No:
Molecular Formula: C7H4N2O2
Molecular Weight: 148.1189

Identification/Properties

Properties
MP:
212-214℃
BP:
370.7°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
148.121g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
148.027g/mol
Monoisotopic Mass:
148.027g/mol
Topological Polar Surface Area:
74A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
206
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:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Cyanopicolinic acid, also known as 5-CPA, is a versatile chemical compound widely used in various chemical synthesis processes. Its primary application lies in its role as a key building block in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.In chemical synthesis, 5-Cyanopicolinic acid acts as a valuable intermediate that can undergo various reactions to yield a range of structurally diverse compounds. One of its notable uses is as a precursor in the synthesis of heterocyclic compounds, particularly pyridine derivatives, which are crucial in drug discovery and development.Furthermore, 5-Cyanopicolinic acid can participate in cross-coupling reactions to form carbon-carbon bonds, making it an essential component in the construction of complex organic molecules. Its ability to undergo substitution reactions, cyclization, and functional group transformations further enhances its utility in organic synthesis.Overall, the strategic placement of the cyano group in the 5 position of the pyridine ring in 5-Cyanopicolinic acid imparts valuable reactivity that enables its widespread application in the synthesis of diverse chemical compounds with significant implications in pharmaceutical and agrochemical industries.