(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)(thiazolidin-3-yl)methanone
97%
Reagent
Code: #129893
CAS Number
2828439-39-8
blur_circular Chemical Specifications
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Molecular Information
Weight
319.23 g/mol
Formula
C₁₆H₂₂BNO₃S
thermostat
Physical Properties
Boiling Point
480.8±40.0 °C(Predicted)
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Storage & Handling
Density
1.18±0.1 g/cm3(Predicted)
Storage
2-8°C, light-proof, inert gas
description Product Description
Used primarily as an intermediate in Suzuki-Miyaura cross-coupling reactions, this compound enables the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group facilitates coupling with aryl halides under palladium catalysis, making it valuable in pharmaceutical and agrochemical research. The presence of a thiazolidine moiety adds potential for biological activity, allowing its use in the development of bioactive compounds and heterocyclic libraries. It is particularly useful in medicinal chemistry for constructing drug-like scaffolds with structural diversity.
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