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CAS 179942-45-1

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6-T-BUTYLDIMETHYSILYLOXY-2-NAPHTHALENEBORONIC ACID

Description:
6-T-Butyldimethylsilyloxy-2-naphthaleneboronic acid is an organoboron compound characterized by the presence of a boronic acid functional group attached to a naphthalene ring, which is further modified by a t-butyldimethylsilyloxy group. This compound typically exhibits properties such as good solubility in organic solvents, making it useful in various organic synthesis applications, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. The boronic acid moiety allows for the formation of stable complexes with diols and other Lewis bases, which can be exploited in sensor applications or as intermediates in the synthesis of more complex molecules. Additionally, the presence of the silyloxy group can enhance the stability and reactivity of the compound under certain conditions. Overall, this compound is valuable in synthetic organic chemistry and materials science, particularly in the development of pharmaceuticals and advanced materials.
Formula:C16H23BO3Si
InChI:InChI=1/C16H23BO3Si/c1-16(2,3)21(4,5)20-15-9-7-12-10-14(17(18)19)8-6-13(12)11-15/h6-11,18-19H,1-5H3
SMILES:CC(C)(C)[Si](C)(C)Oc1ccc2cc(ccc2c1)B(O)O
Synonyms:
  • Akos Brn-0555
  • 6-T-Butyldimethylsilyloxy-2-Naphthyleneboronic Acid
  • 6-T-Butyldimethysilyloxynaphthalene-2-Boronic Acid
  • 6-Tert-Butyldimethylsilyloxy-2-Naphthaleneboronic Acid
  • 6-TBDMSO-2-naphthaleneboronic acid
  • 6-t-Butyldimethylsilyloxy-2-naphthaleneboronic acid
  • 6-T-Butyldimethylsilyloxy-2-Naphtaleneboronic Acid
  • (6-{[Tert-Butyl(Dimethyl)Silyl]Oxy}Naphthalen-2-Yl)Boronic Acid
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