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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)-

3-Pyridinecarboxylic acid, 6-fluoro-, methyl ester

COC(=O)c1ccc(nc1)F Request for Quotation
Chemical Name: 3-Pyridinecarboxylic acid, 6-fluoro-, methyl ester
CAS Number: 1427-06-1
Product Number: AG0034D2(AGN-PC-00NVBC)
Synonyms:
MDL No:
Molecular Formula: C7H6FNO2
Molecular Weight: 155.1264

Identification/Properties

Properties
MP:
48-52 °C
BP:
210.311 °C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
155.128g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
155.038g/mol
Monoisotopic Mass:
155.038g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
151
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#:
-
Hazard Statements:
H302-H319
Precautionary Statements:
P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 6-fluoropyridine-3-carboxylate is a versatile chemical compound that finds widespread application in chemical synthesis processes. As a key building block in organic chemistry, this compound serves as a valuable intermediate for the production of pharmaceuticals, agrochemicals, and various fine chemicals. Its unique structure incorporating a 6-fluoropyridine moiety and an ester group enables it to participate in diverse reactions, leading to the formation of complex molecules with specific properties.In chemical synthesis, Methyl 6-fluoropyridine-3-carboxylate can be utilized for the introduction of both the fluorine and pyridine functionalities into target molecules. This compound serves as a valuable precursor for the synthesis of biologically active compounds, including pharmaceutical drugs and crop protection agents. By undergoing various transformations such as nucleophilic substitutions, esterifications, and hydrogenations, it allows chemists to access a wide range of derivatives with tailored structures and activities.Furthermore, the presence of the ester group in Methyl 6-fluoropyridine-3-carboxylate offers additional versatility in synthetic strategies. Through selective cleavage and functional group interconversions, this compound can be strategically modified to introduce additional functionalities or to facilitate further elaboration of the molecular scaffold. Its compatibility with common reaction conditions and compatibility with a variety of functional groups make it a valuable tool for synthetic chemists seeking to construct complex molecules efficiently.Overall, the strategic placement of the fluoropyridine and ester functionalities in Methyl 6-fluoropyridine-3-carboxylate makes it a valuable and indispensable component in the toolbox of organic chemists engaged in the synthesis of diverse chemical compounds with applications spanning the pharmaceutical, agricultural, and material science industries. Its ability to serve as a starting point for the creation of novel molecules highlights its importance in driving innovation and discovery in the field of organic chemistry.