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CAS 1864003-07-5

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(3S,4R)-1-(tert-butoxycarbonyl)-3-fluoropiperidine-4-carboxylic acid (enantioMer b,87% e.e)

Description:
The chemical substance known as (3S,4R)-1-(tert-butoxycarbonyl)-3-fluoropiperidine-4-carboxylic acid is a chiral compound characterized by its specific stereochemistry, indicated by the (3S,4R) configuration. This compound features a piperidine ring, which is a six-membered nitrogen-containing heterocycle, and includes a tert-butoxycarbonyl (Boc) protecting group that is commonly used in organic synthesis to protect amines. The presence of a fluorine atom at the 3-position of the piperidine ring introduces unique electronic and steric properties, potentially influencing its reactivity and biological activity. The carboxylic acid functional group at the 4-position contributes to its acidity and can participate in various chemical reactions, such as esterification or amidation. The designation of "enantioMer b" and an enantiomeric excess (e.e.) of 87% indicates that this compound is one of two enantiomers, with a predominance of one over the other, which is significant in pharmaceutical applications where chirality can affect the efficacy and safety of drugs. Overall, this compound is of interest in medicinal chemistry and synthetic organic chemistry.
Formula:C11H18FNO4
Synonyms:
  • 1,4-Piperidinedicarboxylic acid, 3-fluoro-, 1-(1,1-dimethylethyl) ester, (3S,4R)-
  • (3S,4R)-1-(tert-butoxycarbonyl)-3-fluoropiperidine-4-carboxylic acid
  • (3S,4R)-1-(tert-butoxycarbonyl)-3-fluoropiperidine-4-carboxylic acid (enantioMer b,87% e.e)
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