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Catalog Number:
20828
CAS Number:
301673-14-3
N -Boc-4-iodo-pipéridine
Purity:
≥ 97% (CG)
Synonym(s):
Ester tert -butylique de l'acide 4-iodo-pipéridine-1-carboxylique, 4-iodopipéridine-1-carboxylate de tert -butyle
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$22.03 /1G
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Product Information

N-Boc-4-iodo-piperidine is a versatile chemical compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound features a tert-butyl carbamate protecting group, which enhances its stability and solubility, making it an ideal candidate for various applications. Its unique structure allows for the introduction of iodine at the 4-position of the piperidine ring, facilitating the development of novel pharmaceuticals and biologically active molecules. Researchers often leverage N-Boc-4-iodo-piperidine in the synthesis of complex organic compounds, particularly in the creation of targeted drug candidates and in the development of new materials.

The compound's ability to undergo various chemical transformations, including nucleophilic substitutions and coupling reactions, makes it a valuable tool for chemists aiming to explore new therapeutic avenues. Its use in the synthesis of iodine-containing compounds is particularly noteworthy, as these derivatives can exhibit enhanced biological activity. With its favorable properties and broad applicability, N-Boc-4-iodo-piperidine stands out as a key intermediate in the pharmaceutical industry and research laboratories.

Synonyms
Ester tert -butylique de l'acide 4-iodo-pipéridine-1-carboxylique, 4-iodopipéridine-1-carboxylate de tert -butyle
CAS Number
301673-14-3
Purity
≥ 97% (CG)
Molecular Formula
C 10 H 18 INO 2
Molecular Weight
311.16
MDL Number
MFCD04115041
PubChem ID
10892302
Melting Point
45-51 °C
Appearance
Solide blanc
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Ester tert -butylique de l'acide 4-iodo-pipéridine-1-carboxylique, 4-iodopipéridine-1-carboxylate de tert -butyle
CAS Number
301673-14-3
Purity
≥ 97% (CG)
Molecular Formula
C 10 H 18 INO 2
Molecular Weight
311.16
MDL Number
MFCD04115041
PubChem ID
10892302
Melting Point
45-51 °C
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

N-Boc-4-iodo-piperidine is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of new drugs targeting neurological disorders.
  • Drug Development: Its unique structure allows for the modification of drug candidates, enhancing their efficacy and selectivity, which is crucial in creating more effective treatments.
  • Material Science: Used in the formulation of advanced materials, particularly in the production of polymers that require specific chemical properties for applications in electronics and coatings.
  • Biochemistry: Acts as a valuable tool in biochemical research, aiding in the study of receptor interactions and enzyme activity, which can lead to breakthroughs in understanding biological processes.
  • Medicinal Chemistry: Its role in the design of novel compounds helps researchers tackle challenges in drug resistance, providing a pathway to develop more potent therapeutic agents.

Citations