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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)-

Methanesulfonyl chloride, bromo-

BrCS(=O)(=O)Cl Request for Quotation
Chemical Name: Methanesulfonyl chloride, bromo-
CAS Number: 10099-08-8
Product Number: AG019V2A(AGN-PC-0NV3WW)
Synonyms:
MDL No:
Molecular Formula: CH2BrClO2S
Molecular Weight: 193.4474

Identification/Properties

Computed Properties
Molecular Weight:
193.439g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
191.865g/mol
Monoisotopic Mass:
191.865g/mol
Topological Polar Surface Area:
42.5A^2
Heavy Atom Count:
6
Formal Charge:
0
Complexity:
110
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


Bromomethanesulfonyl chloride is a versatile compound widely used in chemical synthesis as a sulfonylating agent. It plays a crucial role in the modification of various organic molecules, specifically by introducing sulfonyl functional groups. This reagent is particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals.
Bromomethanesulfonyl chloride is known for its ability to selectively sulfonate nucleophilic sites in molecules, offering precise control over the modification process. It is commonly employed in the synthesis of sulfonamides, sulfonylureas, and other sulfonyl-containing compounds, where its high reactivity and selectivity are advantageous.
Additionally, this compound is essential in the preparation of intermediates for the synthesis of complex organic compounds, providing chemists with a reliable tool for achieving specific structural modifications. Its unique reactivity makes it a valuable resource in medicinal chemistry, enabling the creation of novel drug candidates with enhanced pharmacological properties.
Overall, Bromomethanesulfonyl chloride serves as a versatile and efficient tool in chemical synthesis, enabling the precise functionalization of organic molecules for various applications across the chemical industry.