2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)benzaldehyde
98%
Reagent
Code: #243006
CAS Number
1219936-17-0
science Other reagents with same CAS 1219936-17-0
blur_circular Chemical Specifications
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Molecular Information
Weight
300.08 g/mol
Formula
C₁₄H₁₆BF₃O₃
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Registry Numbers
MDL Number
MFCD18383807
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Storage & Handling
Storage
2-8°C, Inert Gas
description Product Description
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing complex aromatic systems. Its boronate ester group enables efficient coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for developing fluorinated compounds. The presence of both aldehyde and trifluoromethyl groups allows further functionalization, enabling diverse molecular transformations. It is especially useful in the synthesis of bioactive molecules where the trifluoromethyl group enhances metabolic stability and lipophilicity.
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