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CAS 907544-16-5

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tert-butyl (3R,4R)-4-amino-3-fluoro-piperidine-1-carboxylate

Description:
Tert-butyl (3R,4R)-4-amino-3-fluoro-piperidine-1-carboxylate is a chemical compound characterized by its piperidine ring structure, which includes a tert-butyl ester group and an amino group at specific positions. The presence of a fluorine atom at the 3-position and the amino group at the 4-position contributes to its unique reactivity and potential biological activity. This compound is typically used in medicinal chemistry and drug development due to its structural features that may influence pharmacological properties. It is a chiral molecule, with specific stereochemistry at the 3 and 4 positions, which can significantly affect its interaction with biological targets. The tert-butyl group enhances lipophilicity, potentially improving membrane permeability. As with many piperidine derivatives, it may exhibit various biological activities, including effects on neurotransmitter systems. Safety and handling considerations are essential, as with all chemical substances, and appropriate precautions should be taken when working with this compound in a laboratory setting.
Formula:C10H19FN2O2
InChI:InChI=1/C10H19FN2O2/c1-10(2,3)15-9(14)13-5-4-8(12)7(11)6-13/h7-8H,4-6,12H2,1-3H3/t7-,8-/m1/s1
SMILES:CC(C)(C)OC(=O)N1CC[C@H]([C@@H](C1)F)N
Synonyms:
  • tert-butyl (3R,4R)-4-amino-3-fluoropiperidine-1-carboxylate
  • Trans-4-Amino-1-Boc-3-Fluoropiperidine
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