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Catalog Number:
22664
CAS Number:
154775-43-6
Acide 3-(1-Boc-pipéridin-4-yl)propionique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ester tert -butylique de l'acide 4-(2-carboxy-éthyl)pipéridine-1-carboxylique, Acide N -Boc-4-pipéridinepropionique
Documents
$86.23 /100 mg
Taille
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Product Information

3-(1-Boc-piperidin-4-yl)propionic acid is a versatile compound widely utilized in pharmaceutical and chemical research. This compound, also known as Boc-4-piperidyl propionic acid, serves as a crucial building block in the synthesis of various bioactive molecules, particularly in the development of peptide-based therapeutics. Its unique structure, featuring a tert-butoxycarbonyl (Boc) protecting group, allows for selective reactions, making it an ideal candidate for complex organic synthesis. Researchers appreciate its stability and ease of handling, which facilitate efficient reactions in laboratory settings.

In addition to its role in drug discovery, 3-(1-Boc-piperidin-4-yl)propionic acid is employed in the production of intermediates for agrochemicals and specialty chemicals. Its application extends to the development of novel materials and polymers, showcasing its versatility across multiple industries. With its favorable properties and practical applications, this compound is essential for professionals seeking reliable and effective solutions in their research and development endeavors.

Synonyms
Ester tert -butylique de l'acide 4-(2-carboxy-éthyl)pipéridine-1-carboxylique, Acide N -Boc-4-pipéridinepropionique
CAS Number
154775-43-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C 13 H 23 NON 4
Molecular Weight
257.33
MDL Number
MFCD01861212
PubChem ID
1512540
Melting Point
99-109 ?C
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Ester tert -butylique de l'acide 4-(2-carboxy-éthyl)pipéridine-1-carboxylique, Acide N -Boc-4-pipéridinepropionique
CAS Number
154775-43-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C 13 H 23 NON 4
Molecular Weight
257.33
MDL Number
MFCD01861212
PubChem ID
1512540
Melting Point
99-109 ?C
Appearance
Poudre blanche
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-(1-Boc-piperidin-4-yl)propionic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in synthesizing various pharmaceuticals, particularly in the development of analgesics and anti-inflammatory drugs.
  • Peptide Synthesis: It is commonly used in peptide chemistry, where it acts as a building block for creating complex peptide structures, enhancing the efficiency of drug design.
  • Neuroscience Research: The compound's piperidine structure is beneficial in studying neurotransmitter systems, making it valuable for research related to neurological disorders.
  • Bioconjugation Techniques: Its functional groups allow for easy conjugation with biomolecules, facilitating the development of targeted drug delivery systems.
  • Material Science: This chemical can be used to modify polymers, improving their properties for applications in coatings and adhesives.

Citations