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CAS 149716-79-0

:

(S)-N-Boc-pyrrolidin-2-ylboronicacid

Description:
(S)-N-Boc-pyrrolidin-2-ylboronic acid is a boronic acid derivative characterized by the presence of a pyrrolidine ring and a tert-butoxycarbonyl (Boc) protecting group. This compound features a boron atom bonded to a hydroxyl group and an amine, which is part of the pyrrolidine structure. The Boc group serves as a protective moiety for the amine, facilitating various synthetic applications by preventing unwanted reactions during chemical transformations. The chirality of the compound, indicated by the (S) configuration, suggests that it has specific stereochemical properties that can influence its reactivity and interactions in biological systems. Boronic acids are known for their ability to form reversible covalent bonds with diols, making them valuable in medicinal chemistry and materials science. This compound may be utilized in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals, due to its unique structural features and reactivity profile. Its solubility and stability in various solvents can also be important factors in its practical applications.
Formula:C9H18BNO4
InChI:InChI=1S/C9H18BNO4/c1-9(2,3)15-8(12)11-6-4-5-7(11)10(13)14/h7,13-14H,4-6H2,1-3H3/t7-/m1/s1
InChI key:InChIKey=UIIUYLRUCQCTST-SSDOTTSWSA-N
SMILES:C(OC(C)(C)C)(=O)N1[C@@H](B(O)O)CCC1
Synonyms:
  • [(2S)-1-[(tert-Butoxy)carbonyl]pyrrolidin-2-yl]boronic acid
  • 1-(1,1-Dimethylethyl) (2S)-2-borono-1-pyrrolidinecarboxylate
  • 1-Pyrrolidinecarboxylic acid, 2-borono-, 1-(1,1-dimethylethyl) ester, (S)-
  • 1-Pyrrolidinecarboxylic acid, 2-borono-, 1-(1,1-dimethylethyl) ester, (2S)-
  • (S)-N-Boc-pyrrolidin-2-ylboronic acid
  • (S)-(1-(tert-Butoxycarbonyl)pyrrolidin-2-yl)boronic acid
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