Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
41511
CAS Number:
191599-51-6
Ethyl (S)-N-Boc-piperidine-3-carboxylate
Purity:
≥ 95%
Synonym(s):
(S)-(+)-N-Boc-nipecotic acid ethyl ester, (S)-1-(tert-Butoxycarbonyl)-piperidine-3-carboxylicacid ethyl ester, (S)-1-(tert-Butyl) 3-ethyl 1,3-piperidinedicarboxylate, Ethyl (3S)-1-tert-butoxycarbonyl-3-piperidinecarboxylate
Documents
$130.60 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

Ethyl (S)-N-Boc-piperidine-3-carboxylate is a versatile compound widely utilized in the field of organic synthesis and pharmaceutical development. This compound features a Boc (tert-butoxycarbonyl) protecting group, which enhances its stability and reactivity, making it an ideal intermediate in the synthesis of various bioactive molecules. Its chiral nature allows for the production of enantiomerically pure compounds, which is crucial in the development of pharmaceuticals that require specific stereochemistry for efficacy.

Researchers and industry professionals often leverage Ethyl (S)-N-Boc-piperidine-3-carboxylate in the synthesis of piperidine derivatives, which are integral to the development of numerous therapeutic agents, including analgesics and anti-inflammatory drugs. Its unique properties facilitate the formation of complex molecular architectures, thus streamlining the drug discovery process. With its robust applications in medicinal chemistry, this compound stands out as a valuable asset for those engaged in cutting-edge research and development.

Synonyms
(S)-(+)-N-Boc-nipecotic acid ethyl ester, (S)-1-(tert-Butoxycarbonyl)-piperidine-3-carboxylicacid ethyl ester, (S)-1-(tert-Butyl) 3-ethyl 1,3-piperidinedicarboxylate, Ethyl (3S)-1-tert-butoxycarbonyl-3-piperidinecarboxylate
CAS Number
191599-51-6
Purity
≥ 95%
Molecular Formula
C13H23NO4
Molecular Weight
257.33
MDL Number
MFCD07374390
PubChem ID
357727
Melting Point
35 - 40 °C
Appearance
White to light brown solid or liquid
Optical Rotation
[á]22/D = 37 ° (C = 1 in Chloroform)
Conditions
Store at RT
General Information
Synonyms
(S)-(+)-N-Boc-nipecotic acid ethyl ester, (S)-1-(tert-Butoxycarbonyl)-piperidine-3-carboxylicacid ethyl ester, (S)-1-(tert-Butyl) 3-ethyl 1,3-piperidinedicarboxylate, Ethyl (3S)-1-tert-butoxycarbonyl-3-piperidinecarboxylate
CAS Number
191599-51-6
Purity
≥ 95%
Molecular Formula
C13H23NO4
Molecular Weight
257.33
MDL Number
MFCD07374390
PubChem ID
357727
Melting Point
35 - 40 °C
Appearance
White to light brown solid or liquid
Optical Rotation
[á]22/D = 37 ° (C = 1 in Chloroform)
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl (S)-N-Boc-piperidine-3-carboxylate is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting the central nervous system, enhancing drug discovery processes.
  • Peptide Chemistry: It is used in peptide synthesis, allowing for the incorporation of piperidine derivatives, which can improve the stability and efficacy of peptide-based drugs.
  • Ligand Development: The compound is valuable in the development of ligands for metal catalysts, facilitating reactions in organic synthesis and improving reaction yields.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, aiding researchers in understanding neurological disorders and developing potential treatments.
  • Custom Synthesis Services: Many chemical suppliers offer custom synthesis of this compound, providing tailored solutions for specific research needs, which can save time and resources for researchers.

Citations