
CAS 162607-17-2: 5-bromo-2-thienylboronic acid
Formula:C4H4BBrO2S
InChI:InChI=1/C4H4BBrO2S/c6-4-2-1-3(9-4)5(7)8/h1-2,7-8H
SMILES:c1cc(Br)sc1B(O)O
Synonyms:- 5-Bromothiophene-2-boronic acid
- (5-Bromothiophen-2-Yl)Boronic Acid
- 5-Bromo-2-thiopheneboronic acid
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Found 5 products.
2-Bromothiophene-5-boronic acid
CAS:Purity:97.0%Color and Shape:SolidMolecular weight:206.850006103515625-Bromothiophene-2-boronic acid
CAS:5-Bromothiophene-2-boronic acidPurity:97%Molecular weight:206.85g/mol5-Bromo-2-thiopheneboronic Acid (contains varying amounts of Anhydride)
CAS:Formula:C4H4BBrO2SColor and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:206.855-BROMOTHIOPHENE-2-BORONIC ACID
CAS:Formula:C4H4BBrO2SPurity:96%Color and Shape:SolidMolecular weight:206.85345-Bromo-2-thiopheneboronic acid
CAS:5-Bromo-2-thiopheneboronic acid is a boronic acid that can be used for cross-coupling reactions. It has inhibitory properties and can be used to synthesize 4-fluorophenylboronic acid, which is an intermediate of the Suzuki reaction. This product may also be used in the synthesis of boronic acids, which are inhibitors of hormone-sensitive lipase. 5-Bromo-2-thiopheneboronic acid is a chloride salt that does not need to be purified before use. The chloride anion can act as a nucleophile in cross coupling reactions with organoboron compounds or organosilanes. 5-Bromo-2-thiopheneboronic acid also has the ability to inhibit lipid enzymes such as lipase and phospholipase A2 through its ability to bind to and inhibit these enzymes' active sites.Formula:C4H4BBrO2SPurity:Min. 95%Molecular weight:206.85 g/molRef: 3D-FB33368
Discontinued product