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Catalog Number:
22721
CAS Number:
941289-27-6
Acide S- (1-Boc-pipéridin-3-yl)acétique
Purity:
≥ 96%
Synonym(s):
( S -Boc-(3-carboxyméthyl)pipéridine, ( Ester tert -butylique de l'acide S -3-carboxyméthyl-pipéridine-1-carboxylique
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Product Information

(S)-(1-Boc-piperidin-3-yl)acetic acid is a versatile compound widely utilized in pharmaceutical research and development. This chiral building block is particularly valuable for synthesizing various bioactive molecules, including potential therapeutic agents. Its unique structure, featuring a Boc (tert-butyloxycarbonyl) protecting group, enhances its stability and reactivity, making it an ideal candidate for peptide synthesis and medicinal chemistry applications. Researchers appreciate its ability to facilitate the introduction of piperidine moieties into complex organic frameworks, which can lead to the discovery of novel compounds with enhanced biological activity.

In addition to its role in drug discovery, (S)-(1-Boc-piperidin-3-yl)acetic acid is also employed in the synthesis of ligands and catalysts in asymmetric synthesis, showcasing its importance in advancing synthetic methodologies. Its favorable properties, such as solubility and compatibility with various reaction conditions, further bolster its appeal to chemists and researchers. This compound stands out for its potential to streamline the development of new pharmaceuticals, making it a valuable asset in any laboratory focused on innovative drug design.

Synonyms
( S -Boc-(3-carboxyméthyl)pipéridine, ( Ester tert -butylique de l'acide S -3-carboxyméthyl-pipéridine-1-carboxylique
CAS Number
941289-27-6
Purity
≥ 96%
Molecular Formula
C 12 H 21 NON 4
Molecular Weight
243.3
MDL Number
MFCD03094722
PubChem ID
4115028
Appearance
Solide ou poudre blanc à jaune clair
Conditions
Conserver à 0-8°C
General Information
Synonyms
( S -Boc-(3-carboxyméthyl)pipéridine, ( Ester tert -butylique de l'acide S -3-carboxyméthyl-pipéridine-1-carboxylique
CAS Number
941289-27-6
Purity
≥ 96%
Molecular Formula
C 12 H 21 NON 4
Molecular Weight
243.3
MDL Number
MFCD03094722
PubChem ID
4115028
Appearance
Solide ou poudre blanc à jaune clair
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

(S)-(1-Boc-piperidin-3-yl)acetic acid 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 in the development of analgesics and anti-inflammatory drugs.
  • Peptide Chemistry: It is employed in peptide synthesis, where its protective Boc group allows for selective reactions, enhancing the efficiency of creating complex peptide structures.
  • Drug Development: Researchers leverage its unique properties to explore new drug formulations, particularly in the central nervous system (CNS) area, due to its ability to cross the blood-brain barrier.
  • Bioconjugation: The compound is used in bioconjugation processes, facilitating the attachment of drugs to biomolecules, which can improve targeted delivery and reduce side effects.
  • Research on Neurotransmitter Modulation: It is studied for its potential effects on neurotransmitter systems, making it valuable in neuropharmacology research aimed at treating conditions like depression and anxiety.

Citations