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CAS 1052713-48-0

:

1,1-Dimethylethyl N-[(3S,4S)-4-fluoro-3-piperidinyl]carbamate

Description:
1,1-Dimethylethyl N-[(3S,4S)-4-fluoro-3-piperidinyl]carbamate, with the CAS number 1052713-48-0, is a chemical compound characterized by its unique structural features. It contains a carbamate functional group, which is indicative of its potential use in various applications, including pharmaceuticals. The presence of the 4-fluoro-3-piperidinyl moiety suggests that it may exhibit biological activity, possibly as a drug candidate or in medicinal chemistry. The dimethyl group attached to the nitrogen atom contributes to its steric properties, potentially influencing its interaction with biological targets. This compound is likely to be a solid at room temperature, with moderate solubility in organic solvents, and may exhibit stability under standard laboratory conditions. Its specific stereochemistry, denoted by the (3S,4S) configuration, is crucial for its biological activity, as stereoisomers can have significantly different effects in biological systems. Overall, this compound represents a class of molecules that may be of interest in drug development and chemical research.
Formula:C10H19FN2O2
InChI:InChI=1S/C10H19FN2O2/c1-10(2,3)15-9(14)13-8-6-12-5-4-7(8)11/h7-8,12H,4-6H2,1-3H3,(H,13,14)/t7-,8-/m0/s1
InChI key:InChIKey=PHKRFWRGEVHCAT-YUMQZZPRSA-N
SMILES:N(C(OC(C)(C)C)=O)[C@@H]1[C@@H](F)CCNC1
Synonyms:
  • Carbamic acid, N-[(3S,4S)-4-fluoro-3-piperidinyl]-, 1,1-dimethylethyl ester
  • 1,1-Dimethylethyl N-[(3S,4S)-4-fluoro-3-piperidinyl]carbamate
  • (3S,4S)-3-(Boc-amino)-4-fluoropiperidine
  • tert-butyl N-[(3S,4S)-4-fluoropiperidin-3-yl]carbamate
  • (3S,4S)-(4-Fluoro-piperidin-3-yl)-carbamic acid tert-butyl ester
  • tert-butyl ((3S,4S)-4-fluoropiperidin-3-yl)carbamate(WXFC0381)
  • tert-Butyl ((3S,4S)-4-fluoropiperidin-3-yl)carbamate
  • (3S,4S)-3-(BOC-AMINO)-4-FLUOROPIPERIDINERACEMIC-TRANS-3-(BOC-AMINO)-4-FLUOROPIPERIDINE
  • Racemic-Trans-3-(Boc-Amino)-4-Fluoropiperidine
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