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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, 6-(bromomethyl)-, ethyl ester

CCOC(=O)c1cccc(n1)CBr Request for Quotation
Chemical Name: 2-Pyridinecarboxylic acid, 6-(bromomethyl)-, ethyl ester
CAS Number: 97278-44-9
Product Number: AG005ZVB(AGN-PC-03Y9FN)
Synonyms:
MDL No:
Molecular Formula: C9H10BrNO2
Molecular Weight: 244.0852

Identification/Properties

Properties
Storage:
-10 ℃;
Form:
Liquid
Computed Properties
Molecular Weight:
244.088g/mol
XLogP3:
2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
242.989g/mol
Monoisotopic Mass:
242.989g/mol
Topological Polar Surface Area:
39.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
175
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 6-(bromomethyl)picolinate is a versatile compound widely used in chemical synthesis. This specialized chemical plays a crucial role in various reactions, particularly in the field of organic chemistry. Its unique structural properties make it a valuable building block for creating complex molecules and conducting intricate transformations in the laboratory.One of the key applications of ethyl 6-(bromomethyl)picolinate is in the synthesis of pharmaceuticals and agrochemicals. By acting as a halogenated intermediate, this compound enables the introduction of a bromomethyl group into target molecules, which can significantly enhance their biological activity or modify their physicochemical properties. This strategic functional group manipulation is essential in drug discovery and development, as it allows chemists to tailor the properties of a molecule to achieve desired pharmacological effects.Furthermore, ethyl 6-(bromomethyl)picolinate serves as a valuable reagent in the preparation of diverse chemical libraries for high-throughput screening in medicinal chemistry research. Its ability to undergo various reactions, such as substitution, cross-coupling, or functional group interconversion, provides researchers with a versatile tool for designing and synthesizing novel compounds with potential therapeutic applications.In summary, Ethyl 6-(bromomethyl)picolinate is a key intermediate in chemical synthesis, particularly in the pharmaceutical and agrochemical industries. Its role in building complex molecules and modifying functional groups makes it an indispensable component in the arsenal of synthetic chemists seeking to develop innovative compounds for various applications.