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

Catalog Number:
16102
CAS Number:
88495-54-9
Ácido Boc-L-nipecótico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Boc-L-Nip-OH, Ácido Boc-( S -piperidina-3-carboxílico
Hazmat
Documents
$18.53 /1G
Tamaño
Request Bulk Quote
Product Information

Boc-L-nipecotic acid is a valuable compound widely utilized in the field of medicinal chemistry and pharmaceutical research. This amino acid derivative, characterized by its Boc (tert-butyloxycarbonyl) protecting group, plays a crucial role in the synthesis of various bioactive molecules. Its unique structure allows for the selective modification of piperidine derivatives, making it an essential building block in the development of novel therapeutics. Researchers often leverage Boc-L-nipecotic acid in the design of compounds targeting neurological disorders, as its structural features can enhance bioavailability and receptor affinity.

In addition to its applications in drug development, Boc-L-nipecotic acid is also employed in peptide synthesis, where it serves as a key intermediate for creating complex peptide sequences. Its stability and ease of handling make it a preferred choice among chemists, facilitating efficient synthesis processes. The compound's versatility and effectiveness in enhancing the pharmacological properties of various agents underscore its significance in both academic and industrial settings, making it an indispensable tool for researchers focused on advancing therapeutic innovations.

Synonyms
Boc-L-Nip-OH, Ácido Boc-( S -piperidina-3-carboxílico
CAS Number
88495-54-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 11 H 19 N.º 4
Molecular Weight
229.27
PubChem ID
2735647
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Boc-L-Nip-OH, Ácido Boc-( S -piperidina-3-carboxílico
CAS Number
88495-54-9
Purity
≥ 98 % (HPLC)
Molecular Formula
C 11 H 19 N.º 4
Molecular Weight
229.27
PubChem ID
2735647
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Boc-L-nipecotic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions and enhancing the yield of desired products.
  • Drug Development: It plays a crucial role in the design of novel pharmaceuticals, particularly in the development of compounds targeting neurological disorders.
  • Biochemical Research: Researchers use it to study the interactions of amino acids and their derivatives, which is essential for understanding protein structure and function.
  • Analytical Chemistry: The compound is employed in various analytical techniques, including chromatography, to separate and identify complex mixtures.
  • Material Science: Its unique properties make it useful in the formulation of advanced materials, such as polymers, that require specific chemical functionalities.

Citas