🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
43455
CAS Number:
142851-03-4
1-( tert -butoxycarbonyl)-4-pipéridinecarboxylate d'éthyle
Grade:
Ester 1-tert-butyle et 4-éthyle de l'acide pipéridine-1,4-dicarboxylique
Purity:
≥ 97% (CG)
Synonym(s):
Ester éthylique de l'acide 1-( tert- butoxycarbonyl)-4-pipéridinecarboxylique, 1-Boc-4-pipéridinecarboxylate d'éthyle, Ester éthylique de l'acide 1-Boc-4-pipéridinecarboxylique, 1- tert -butyle 4-éthyl pipéridine-1,4-dicarboxylate
Documents
$36.35 /5G
Taille
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
Ester éthylique de l'acide 1-( tert- butoxycarbonyl)-4-pipéridinecarboxylique, 1-Boc-4-pipéridinecarboxylate d'éthyle, Ester éthylique de l'acide 1-Boc-4-pipéridinecarboxylique, 1- tert -butyle 4-éthyl pipéridine-1,4-dicarboxylate
CAS Number
142851-03-4
Purity
≥ 97% (CG)
Grade
Ester 1-tert-butyle et 4-éthyle de l'acide pipéridine-1,4-dicarboxylique
Molecular Formula
C 13 H 23 NON 4
Molecular Weight
257.33
MDL Number
MFCD01763998
PubChem ID
2758812
Density
1.05
Appearance
Liquide incolore à jaune clair à orange clair, limpide à légèrement trouble l
Boiling Point
140 °C/0,098 mmHg
Refractive Index
n20D 1.46
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
Ester éthylique de l'acide 1-( tert- butoxycarbonyl)-4-pipéridinecarboxylique, 1-Boc-4-pipéridinecarboxylate d'éthyle, Ester éthylique de l'acide 1-Boc-4-pipéridinecarboxylique, 1- tert -butyle 4-éthyl pipéridine-1,4-dicarboxylate
CAS Number
142851-03-4
Purity
≥ 97% (CG)
Grade
Ester 1-tert-butyle et 4-éthyle de l'acide pipéridine-1,4-dicarboxylique
Molecular Formula
C 13 H 23 NON 4
Molecular Weight
257.33
MDL Number
MFCD01763998
PubChem ID
2758812
Density
1.05
Appearance
Liquide incolore à jaune clair à orange clair, limpide à légèrement trouble l
Boiling Point
140 °C/0,098 mmHg
Refractive Index
n20D 1.46
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
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.

Citations