CAS NO:162607-17-2 5-bromothiophene-2-boronic acid
CAS NO:162607-17-2 NAME:5-bromothiophene-2-boronic acid MF：C4H4BBrO2S MW：206.85 Purity:97%min Appearance:White to Light yellow powder COA:Provide Sample:Negotiable
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Life Science Chemicals
Pharmaceutical Intermediates
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Product introduction
| PRODUCT NAME | 5-bromothiophene-2-boronic acid |
| CAS NO | 51372-93-1 |
| MP | 95-100 °C(lit.) |
| BP | 342.3±52.0 °C(Predicted) |
| DENSITY | 1.87±0.1 g/cm3(Predicted) |
| STORAGE | 2-8°C |
| DELIVERY | 2-3DAYS |
| PACKAGE | According client's request |
Description of CAS NO:162607-17-2 5-bromothiophene-2-boronic acid
5-Bromo-2-thiopheneboronic acid CAS NO:162607-17-2 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.
Applications of CAS NO:162607-17-2 5-bromothiophene-2-boronic acid
REACTANT INVOLVED IN: SUZUKI COUPLING REACTIONS FOR THE SYNTHESIS OF BENZOTRIAZOLE-CONTAINING ORGANIC SENSITIZERS AND MESO-POLYARYLAMIDE-BODIPY HYBRIDS. SUZUKI-MIYAURA COUPLING FOR THE SYNTHESIS OF RATANHINE. MICROWAVE-ASSISTED SONOGASHIRA REACTIONS FOR THE SYNTHESIS OF ETHYNYLARYLBORONATES
OTHER NOTES: CONTAINS VARYING AMOUNTS OF ANHYDRIDE
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