(4-(Thiazolidine-3-carbonyl)phenyl)boronic acid
98%
Reagent
Code: #243583
CAS Number
850589-33-2
science Other reagents with same CAS 850589-33-2
blur_circular Chemical Specifications
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Molecular Information
Weight
237.08 g/mol
Formula
C₁₀H₁₂BNO₃S
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Registry Numbers
MDL Number
MFCD04115680
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Storage & Handling
Storage
2-8°C, Inert Gas
description Product Description
Used in organic synthesis as a building block for pharmaceuticals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation, making it valuable in drug discovery and development. The thiazolidine moiety can contribute to biological activity, allowing incorporation into molecules with potential antimicrobial or antidiabetic properties. Also applied in the synthesis of sensors and functional materials due to its selective binding and reactivity.
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