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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-bromo-5-propan-2-ylsulfonylpyridine

Brc1ccc(cn1)S(=O)(=O)C(C)C Request for Quotation
Chemical Name: 2-bromo-5-propan-2-ylsulfonylpyridine
CAS Number: 1245648-96-7
Product Number: AG000MC7(AGN-PC-09MQY7)
Synonyms:
MDL No:
Molecular Formula: C8H10BrNO2S
Molecular Weight: 264.1395

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-5-(isopropylsulfonyl)pyridine is a versatile compound widely utilized in chemical synthesis as a key building block for the preparation of various functionalized molecules. This compound serves as a valuable intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its unique reactivity and structural properties. In organic synthesis, 2-Bromo-5-(isopropylsulfonyl)pyridine can participate in a variety of reactions such as nucleophilic substitution, Suzuki-Miyaura coupling, and palladium-catalyzed cross-coupling reactions to introduce diverse functional groups into organic molecules. Its ability to readily undergo selective transformations makes it a valuable tool for the construction of complex molecular architectures in the laboratory setting. Furthermore, the presence of the bromo and sulfonyl groups in 2-Bromo-5-(isopropylsulfonyl)pyridine imparts it with desirable reactivity profiles, enabling chemists to carry out controlled and efficient synthetic routes towards the targeted compounds.