CAS 50450-21-0
:bromo(dimethyl)sulfonium bromide
Description:
Bromo(dimethyl)sulfonium bromide, with the CAS number 50450-21-0, is a quaternary ammonium salt characterized by its sulfonium ion structure. It typically appears as a white to off-white crystalline solid and is soluble in polar solvents such as water and alcohols. This compound features a dimethylsulfonium cation, which is positively charged, and a bromide anion, contributing to its ionic nature. It is often used as a reagent in organic synthesis, particularly in alkylation reactions and as a source of the dimethylsulfonium ion. The presence of bromine in both the cation and anion enhances its reactivity, making it useful in various chemical transformations. Additionally, bromo(dimethyl)sulfonium bromide can exhibit properties such as hygroscopicity, meaning it can absorb moisture from the air. Safety precautions should be taken when handling this compound, as it may pose health risks if inhaled or ingested. Overall, its unique structure and reactivity make it a valuable tool in synthetic organic chemistry.
Formula:C2H6Br2S
InChI:InChI=1/C2H6BrS.BrH/c1-4(2)3;/h1-2H3;1H/q+1;/p-1
Synonyms:- Sulfonium, Bromodimethyl-, Bromide (1:1)
- Bromo(dimethyl)sulfonium bromide
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Found 6 products.
Bromodimethylsulfonium bromide
CAS:Formula:C2H6Br2SPurity:95%Color and Shape:SolidMolecular weight:221.9420Bromodimethylsulfonium bromide
CAS:<p>Bromodimethylsulfonium bromide</p>Purity:98%Molecular weight:221.94g/molBromodimethylsulfonium bromide
CAS:<p>Bromodimethylsulfonium bromide</p>Purity:98%Molecular weight:221.94g/molBromodimethylsulfonium Bromide
CAS:Formula:C2H6Br2SPurity:>98.0%(T)Color and Shape:Light yellow to Brown powder to crystalMolecular weight:221.94Bromodimethylsulfonium bromide
CAS:<p>Bromodimethylsulfonium bromide is a chemical that has been used as a diagnostic agent in the diagnosis of leukemia. It is also used for the treatment of cancer, although it has shown to be ineffective against some resistant mutants. Bromodimethylsulfonium bromide is an unsymmetrical ion with one proton and one bromine atom. It reacts with amines to form an alkylammonium cation, which in turn reacts with nucleophiles such as water or alcohols to form a glycosidic bond. This reaction is responsible for the tissue culture growth inhibition seen in cells treated with this compound. Bromodimethylsulfonium bromide also inhibits fatty acid synthesis by preventing the enzyme acyl-CoA synthase from functioning properly, which leads to decreased levels of cellular energy production. Bromodimethylsulfonium bromide's fluorescence properties can be observed in tissue culture</p>Formula:C2H6Br2SPurity:Min. 95%Molecular weight:221.94 g/mol




