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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-Pyridinesulfonylchloride, 6-bromo-

Brc1cccc(n1)S(=O)(=O)Cl Request for Quotation
Chemical Name: 2-Pyridinesulfonylchloride, 6-bromo-
CAS Number: 912934-77-1
Product Number: AG0038JL(AGN-PC-078TC0)
Synonyms:
MDL No:
Molecular Formula: C5H3BrClNO2S
Molecular Weight: 256.5048

Identification/Properties

Computed Properties
Molecular Weight:
256.498g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
254.876g/mol
Monoisotopic Mass:
254.876g/mol
Topological Polar Surface Area:
55.4A^2
Heavy Atom Count:
11
Formal Charge:
0
Complexity:
225
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:
Danger
UN#:
3265
Hazard Statements:
H314
Precautionary Statements:
P260-P280-P303+P361+P353-P301+P330+P331-P304+P340+P310-P305+P351+P338+P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


6-Bromo-2-pyridinesulfonyl chloride is a versatile building block in chemical synthesis due to its unique reactivity and functional groups. Its application lies primarily in the field of organic chemistry as a key intermediate for the synthesis of various pharmaceuticals, agrochemicals, and materials.It serves as a valuable tool in the preparation of heterocyclic compounds, which are vital in drug discovery and development. The reactivity of the sulfonyl chloride group allows for the introduction of the 6-bromo-2-pyridine moiety into complex molecular structures, enabling the creation of novel compounds with diverse biological activities.Additionally, 6-Bromo-2-pyridinesulfonyl chloride is widely utilized in the construction of molecular scaffolds for the design of new synthetic methodologies. Its ability to participate in cross-coupling reactions, substitution reactions, and other transformations makes it a valuable reagent for the synthesis of libraries of compounds for screening purposes.Overall, the versatility and reactivity of 6-Bromo-2-pyridinesulfonyl chloride make it a valuable tool for chemists engaged in the field of chemical synthesis, enabling the efficient and strategic construction of complex molecules with potential applications in various sectors of the chemical industry.