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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)-

6-Cyano-2-pyridine carboxylic acid methyl ester

COC(=O)c1cccc(n1)C#N Request for Quotation
Chemical Name: 6-Cyano-2-pyridine carboxylic acid methyl ester
CAS Number: 98436-83-0
Product Number: AG00IK38(AGN-PC-05IV1F)
Synonyms:
MDL No: MFCD07367924
Molecular Formula: C8H6N2O2
Molecular Weight: 162.1454

Identification/Properties

Computed Properties
Molecular Weight:
162.148g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
162.043g/mol
Monoisotopic Mass:
162.043g/mol
Topological Polar Surface Area:
63A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
218
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


Methyl 6-cyanopicolinate, also known as methyl 6-cyanopyridine-2-carboxylate, is a key intermediate commonly used in chemical synthesis processes. This compound plays a crucial role in the production of various pharmaceuticals, agrochemicals, and fine chemicals due to its versatile chemical properties.In chemical synthesis, Methyl 6-cyanopicolinate serves as a valuable building block for the preparation of heterocyclic compounds and complex molecules. Its unique structural features make it a preferred reagent in the formation of substituted pyridines, which are essential components in the development of pharmaceutical drugs and biologically active compounds.Furthermore, the reactivity of Methyl 6-cyanopicolinate allows for the introduction of functional groups at specific positions, enabling chemists to tailor the structure of target molecules for desired properties. This compound's involvement in cross-coupling reactions, nucleophilic substitutions, and other transformation processes showcases its significance in the synthesis of diverse chemical entities.Overall, Methyl 6-cyanopicolinate's pivotal role in chemical synthesis lies in its ability to act as a versatile precursor for the construction of complex organic molecules with potential applications across various industries.