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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)-

Pyridine, 5-bromo-2-(methylsulfonyl)-

Brc1ccc(nc1)S(=O)(=O)C Request for Quotation
Chemical Name: Pyridine, 5-bromo-2-(methylsulfonyl)-
CAS Number: 98626-95-0
Product Number: AG005U1P(AGN-PC-00MK0A)
Synonyms:
MDL No:
Molecular Formula: C6H6BrNO2S
Molecular Weight: 236.0863

Identification/Properties

Properties
MP:
95-96℃
BP:
366.287°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
236.083g/mol
XLogP3:
1.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
234.93g/mol
Monoisotopic Mass:
234.93g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
221
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:
H319-H302
Precautionary Statements:
P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-2-(methylsulfonyl)pyridine, also known as $name$, serves as a versatile building block in chemical synthesis due to its unique structural properties. This compound is commonly utilized as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals.One prominent application of 5-Bromo-2-(methylsulfonyl)pyridine is in the development of novel pharmaceutical compounds. Its reactive bromine functional group allows for efficient coupling reactions with various nucleophiles, enabling the creation of diverse molecular structures with potential biological activity. Additionally, the presence of the methylsulfonyl moiety enhances the compound's stability and solubility, making it suitable for further modifications in drug discovery processes.Furthermore, 5-Bromo-2-(methylsulfonyl)pyridine plays a crucial role in the synthesis of agrochemicals by serving as a key precursor in the production of pesticides, herbicides, and fungicides. Its pyridine ring confers specific chemical reactivity, enabling the introduction of functional groups that are essential for pesticidal activity.In the realm of fine chemicals, this compound is valued for its utility in the construction of complex organic molecules with tailored properties. Its strategic placement of functional groups allows for precise structural modifications, making it a valuable building block in the synthesis of specialty chemicals used in various industries.Overall, the strategic positioning of the bromine and methylsulfonyl groups in 5-Bromo-2-(methylsulfonyl)pyridine offers synthetic chemists a powerful tool for designing and synthesizing novel molecules with diverse applications in pharmaceuticals, agrochemicals, and fine chemicals.