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CAS 1887223-13-3

:

(5-((TERT-BUTOXYCARBONYL)AMINO)-2-METHYLPYRIDIN-3-YL)BORONIC ACID PINACOL ESTER

Description:
(5-((Tert-butoxycarbonyl)amino)-2-methylpyridin-3-yl)boronic acid pinacol ester is a boronic acid derivative characterized by the presence of a boron atom bonded to a pinacol ester group and an amino-substituted pyridine ring. This compound typically exhibits properties associated with boronic acids, such as the ability to form reversible covalent bonds with diols, making it useful in various organic synthesis applications, particularly in Suzuki coupling reactions. The tert-butoxycarbonyl (Boc) group serves as a protective group for the amine, enhancing the compound's stability and facilitating selective reactions. The presence of the methyl group on the pyridine ring can influence the compound's reactivity and solubility. Generally, boronic acid derivatives are known for their moderate solubility in organic solvents and can be sensitive to moisture and air, necessitating careful handling and storage. This compound may find applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its potential to interact with biological targets through boron-mediated interactions.
Formula:C17H27BN2O4
Synonyms:
  • tert-butyl (6-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl)carbamate
  • (2E)-3-(5-methyl-47-furyl)acrylic acid
  • tert-Butyl N-[6-methyl-5-(tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl]carbamate
  • (5-((TERT-BUTOXYCARBONYL)AMINO)-2-METHYLPYRIDIN-3-YL)BORONIC ACID PINACOL ESTER
  • tert-butyl 3-allyl-3-hydroxyazetidine-34-carboxylate
  • Carbamic acid, N-[6-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-pyridinyl]-, 1,1-dimethylethyl ester
  • tert-butyl N-[6-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-3-yl]carbamate
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