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Catalog Number:
26135
CAS Number:
165528-81-4
4-(2-Boc-aminoéthyl)pipéridine
Purity:
≥ 95 % (RMN)
Synonym(s):
Ester tert -butylique de l'acide (2-pipéridin-4-yl-éthyl)-carbamique
Documents
$27.94 /250 mg
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Product Information

4-(2-Boc-aminoethyl)piperidine is a versatile chemical compound widely utilized in pharmaceutical research and development. This compound, known for its stability and ease of handling, serves as a crucial intermediate in the synthesis of various bioactive molecules. Its unique structure, featuring a tert-butyl carbamate protecting group, allows for selective reactions, making it an ideal candidate for the development of novel therapeutic agents. Researchers appreciate its role in enhancing the solubility and bioavailability of drug candidates, particularly in the design of piperidine-based pharmaceuticals.

In addition to its applications in medicinal chemistry, 4-(2-Boc-aminoethyl)piperidine is also valuable in the field of materials science, where it can be employed in the synthesis of polymers and other advanced materials. Its ability to undergo diverse chemical transformations opens up possibilities for creating innovative compounds with tailored properties. This compound stands out for its compatibility with various reaction conditions, making it a preferred choice for both academic and industrial applications.

Synonyms
Ester tert -butylique de l'acide (2-pipéridin-4-yl-éthyl)-carbamique
CAS Number
165528-81-4
Purity
≥ 95 % (RMN)
Molecular Formula
C12H24N2O2
Molecular Weight
228.33
MDL Number
MFCD01318373
PubChem ID
1501849
Appearance
Solide blanc
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Ester tert -butylique de l'acide (2-pipéridin-4-yl-éthyl)-carbamique
CAS Number
165528-81-4
Purity
≥ 95 % (RMN)
Molecular Formula
C12H24N2O2
Molecular Weight
228.33
MDL Number
MFCD01318373
PubChem ID
1501849
Appearance
Solide blanc
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

4-(2-Boc-aminoethyl)piperidine is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as an important building block in the synthesis of various pharmaceuticals, enabling researchers to create complex molecules with enhanced biological activity.
  • Drug Development: It is frequently used in the development of new drugs targeting neurological disorders, providing a framework for designing compounds that can effectively cross the blood-brain barrier.
  • Bioconjugation: The compound is valuable in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the efficacy of targeted therapies.
  • Material Science: In polymer chemistry, it acts as a modifier to improve the properties of polymers, leading to materials with better mechanical strength and thermal stability.
  • Research in Neuroscience: It is utilized in studies related to neurotransmitter systems, aiding in the exploration of new treatments for conditions like depression and anxiety.

Citations