CAS 2121514-99-4
:B-[2,6-Dimethoxy-5-(trimethylsilyl)-3-pyridinyl]boronic acid
Description:
B-[2,6-Dimethoxy-5-(trimethylsilyl)-3-pyridinyl]boronic acid is an organoboron compound characterized by the presence of a boronic acid functional group, which is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and medicinal chemistry. The compound features a pyridine ring substituted with two methoxy groups and a trimethylsilyl group, which can influence its solubility and reactivity. The presence of the boronic acid moiety allows for participation in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is pivotal in the formation of carbon-carbon bonds. Additionally, the trimethylsilyl group can enhance the stability and lipophilicity of the compound, potentially affecting its biological activity and interaction with other molecules. Overall, this compound exemplifies the versatility of boronic acids in synthetic chemistry and their role in the development of pharmaceuticals and agrochemicals.
Formula:C10H18BNO4Si
InChI:InChI=1S/C10H18BNO4Si/c1-15-9-7(11(13)14)6-8(17(3,4)5)10(12-9)16-2/h6,13-14H,1-5H3
InChI key:InChIKey=YWXBHJRUYUJTGE-UHFFFAOYSA-N
SMILES:O(C)C1=C([Si](C)(C)C)C=C(B(O)O)C(OC)=N1
Synonyms:- Boronic acid, B-[2,6-dimethoxy-5-(trimethylsilyl)-3-pyridinyl]-
- B-[2,6-Dimethoxy-5-(trimethylsilyl)-3-pyridinyl]boronic acid
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