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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-(methylsulfonyl)-, ethyl ester

CCOC(=O)c1ccc(cn1)S(=O)(=O)C Request for Quotation
Chemical Name: 2-Pyridinecarboxylic acid, 5-(methylsulfonyl)-, ethyl ester
CAS Number: 918967-32-5
Product Number: AG003QBV(AGN-PC-09SGBG)
Synonyms:
MDL No: MFCD18071044
Molecular Formula: C9H11NO4S
Molecular Weight: 229.2529

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P264-P270-P301+P312-P330
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


Ethyl 5-(Methylsulfonyl)pyridine-2-carboxylate is a versatile compound commonly used in chemical synthesis due to its unique reactivity and functionality. This compound serves as an important building block in the synthesis of various organic compounds, pharmaceuticals, and agrochemicals.In chemical synthesis, Ethyl 5-(Methylsulfonyl)pyridine-2-carboxylate is often employed as a key intermediate in the preparation of complex molecules. Its sulfur-containing moiety provides a handle for further derivatization, allowing chemists to introduce additional functional groups or modify its structure to tailor properties for specific applications. Furthermore, the pyridine ring in Ethyl 5-(Methylsulfonyl)pyridine-2-carboxylate imparts aromatic character and can participate in a range of chemical reactions including nucleophilic substitutions, cross-coupling reactions, and cycloadditions. This versatility makes it a valuable component in the creation of diverse molecular scaffolds with varied biological activities and physical properties.