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CAS 1040281-97-7

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3-Chlorothiophene-2-boronic acid pinacol ester

Description:
3-Chlorothiophene-2-boronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid moiety and a chlorothiophene ring. This compound typically exhibits a white to off-white solid form and is soluble in organic solvents such as dichloromethane and tetrahydrofuran. The presence of the boronic acid functional group allows for participation in Suzuki-Miyaura cross-coupling reactions, making it valuable in organic synthesis, particularly in the formation of carbon-carbon bonds. The chlorothiophene structure contributes to its reactivity and potential applications in the development of pharmaceuticals and agrochemicals. Additionally, the pinacol ester formation enhances stability and solubility, facilitating its use in various chemical transformations. As with many organoboron compounds, it is important to handle this substance with care, as it may be sensitive to moisture and air, which can affect its reactivity and stability. Overall, 3-Chlorothiophene-2-boronic acid pinacol ester is a versatile building block in synthetic organic chemistry.
Formula:C10H14BClO2S
InChI:InChI=1/C10H14BClO2S/c1-9(2)10(3,4)14-11(13-9)8-7(12)5-6-15-8/h5-6H,1-4H3
SMILES:CC1(C)C(C)(C)OB(c2c(ccs2)Cl)O1
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