🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
43455
CAS Number:
142851-03-4
1-( terc- butoxicarbonil)-4-piperidinacarboxilato de etilo
Grade:
Éster 1-terc-butílico 4-etílico del ácido piperidin-1,4-dicarboxílico
Purity:
≥ 97% (GC)
Synonym(s):
Éster etílico del ácido 1-( terc- butoxicarbonil)-4-piperidinacarboxílico, 1-Boc-4-piperidinacarboxilato de etilo, Éster etílico del ácido 1-Boc-4-piperidinacarboxílico, 1- tert -butil 4-etil piperidina-1,4-dicarboxilato
Documents
$36.35 /5G
Tamaño
Request Bulk Quote
Product Information

Ethyl 1-(tert-butoxycarbonyl)-4-piperidinecarboxylate is a versatile compound widely utilized in organic synthesis and pharmaceutical research. This compound, also known as Ethyl 4-piperidinecarboxylate, is characterized by its unique structure that allows for the introduction of functional groups, making it an essential building block in the development of various bioactive molecules. Its stability and reactivity make it particularly valuable in the synthesis of piperidine derivatives, which are often employed in the production of pharmaceuticals, agrochemicals, and other fine chemicals.

Researchers appreciate Ethyl 1-(tert-butoxycarbonyl)-4-piperidinecarboxylate for its ability to facilitate complex reactions while maintaining high yields. Its application extends to the synthesis of potential drug candidates, where it serves as a precursor in the formation of compounds with significant therapeutic potential. The compound's favorable properties, such as solubility and compatibility with various reaction conditions, further enhance its appeal in both academic and industrial settings, making it a preferred choice for chemists looking to innovate in drug design and development.

Synonyms
Éster etílico del ácido 1-( terc- butoxicarbonil)-4-piperidinacarboxílico, 1-Boc-4-piperidinacarboxilato de etilo, Éster etílico del ácido 1-Boc-4-piperidinacarboxílico, 1- tert -butil 4-etil piperidina-1,4-dicarboxilato
CAS Number
142851-03-4
Purity
≥ 97% (GC)
Grade
Éster 1-terc-butílico 4-etílico del ácido piperidin-1,4-dicarboxílico
Molecular Formula
C13H23NO4
Molecular Weight
257.33
MDL Number
MFCD01763998
PubChem ID
2758812
Density
1.05
Appearance
Líquido transparente incoloro a amarillo claro a naranja claro a ligeramente turbio.
Boiling Point
140 °C/0,098 mmHg
Refractive Index
n20D 1,46
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Éster etílico del ácido 1-( terc- butoxicarbonil)-4-piperidinacarboxílico, 1-Boc-4-piperidinacarboxilato de etilo, Éster etílico del ácido 1-Boc-4-piperidinacarboxílico, 1- tert -butil 4-etil piperidina-1,4-dicarboxilato
CAS Number
142851-03-4
Purity
≥ 97% (GC)
Grade
Éster 1-terc-butílico 4-etílico del ácido piperidin-1,4-dicarboxílico
Molecular Formula
C13H23NO4
Molecular Weight
257.33
MDL Number
MFCD01763998
PubChem ID
2758812
Density
1.05
Appearance
Líquido transparente incoloro a amarillo claro a naranja claro a ligeramente turbio.
Boiling Point
140 °C/0,098 mmHg
Refractive Index
n20D 1,46
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 1-(tert-butoxycarbonyl)-4-piperidinecarboxylate is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders.
  • Organic Synthesis: It is employed in the preparation of complex organic molecules, allowing chemists to create compounds with specific functional groups efficiently.
  • Peptide Synthesis: This chemical is used in the protection of amino acids during peptide synthesis, enhancing the yield and purity of the final products.
  • Material Science: It finds application in developing polymers and materials with tailored properties, which can be beneficial in creating advanced coatings and adhesives.
  • Research in Medicinal Chemistry: The compound is valuable in exploring structure-activity relationships, aiding researchers in designing more effective drug candidates.

Citas