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CAS 51077-14-6

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(S)-N-BOC-Azetidine carboxylic acid

Description:
(S)-N-BOC-Azetidine carboxylic acid is a chiral compound characterized by its azetidine ring structure, which is a four-membered cyclic amine. The "N-BOC" designation indicates that the amine group is protected by a tert-butyloxycarbonyl (BOC) group, enhancing its stability and facilitating further chemical reactions. This compound features a carboxylic acid functional group, contributing to its acidity and reactivity. The presence of chirality in the (S) configuration implies that it can exist as two enantiomers, with distinct properties and biological activities. Typically, compounds like (S)-N-BOC-Azetidine carboxylic acid are utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to their ability to serve as intermediates in the synthesis of more complex molecules. Its solubility and stability in various solvents make it a versatile reagent in chemical reactions. As with many azetidine derivatives, it may exhibit interesting biological properties, warranting further investigation in medicinal chemistry.
Formula:C9H14NO4
InChI:InChI=1/C9H15NO4/c1-9(2,3)14-8(13)10-5-4-6(10)7(11)12/h6H,4-5H2,1-3H3,(H,11,12)/p-1/t6-/m0/s1
SMILES:CC(C)(C)OC(=O)N1CC[C@H]1C(=O)[O-]
Synonyms:
  • (S)-N-tert-Butoxycarbonyl-azetidine-2-carboxylic acid
  • (S)-N-BOC-Azetidine-2-carboxylic acid
  • 1-Boc-L-azetidine-2-carboxylic acid
  • (2S)-1-(tert-butoxycarbonyl)azetidine-2-carboxylic acid
  • (2S)-1-(tert-butoxycarbonyl)azetidine-2-carboxylate
  • (S)-1-Boc-2-azetidinecarboxylic acid
  • (2S)-1-[(tert-butoxy)carbonyl]azetidine-2-carboxylic acid
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