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Catalog Number:
29668
CAS Number:
913542-81-1
Ácido Fmoc-4-(4-bromofenil)-piperidina-4-carboxílico
Purity:
≥ 98 % (HPLC)
Documents
$93.14 /100 mg
Tamaño
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Product Information

Fmoc-4-(4-bromophenyl)-piperidine-4-carboxylic acid is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound is particularly valued for its role as a building block in the synthesis of peptide and protein derivatives, where the Fmoc (9-fluorenylmethoxycarbonyl) protecting group facilitates selective deprotection during peptide synthesis. Its unique structure, featuring a bromophenyl moiety, enhances its reactivity and compatibility with various coupling reactions, making it an essential tool for researchers focused on developing novel therapeutic agents.

In addition to its applications in peptide synthesis, Fmoc-4-(4-bromophenyl)-piperidine-4-carboxylic acid is also explored for its potential in drug discovery and development, particularly in the design of inhibitors and other bioactive compounds. Its ability to serve as a versatile intermediate allows chemists to create diverse molecular architectures, thereby expanding the possibilities for innovative drug candidates. With its robust performance in synthetic applications, this compound stands out as a preferred choice for professionals aiming to streamline their research and development processes.

CAS Number
913542-81-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C27H24BrNO4
Molecular Weight
506.4
MDL Number
MFCD11226815
PubChem ID
45356722
Melting Point
182-189 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
913542-81-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C27H24BrNO4
Molecular Weight
506.4
MDL Number
MFCD11226815
PubChem ID
45356722
Melting Point
182-189 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-4-(4-bromophenyl)-piperidine-4-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: Its unique structure is beneficial in designing novel pharmaceutical compounds, particularly in the development of targeted therapies for various diseases.
  • Bioconjugation: The chemical is used in bioconjugation techniques, enabling the attachment of biomolecules to surfaces or other molecules, which is crucial in creating effective drug delivery systems.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, particularly in the synthesis of compounds that can modulate receptor activity, aiding in the understanding of neurological disorders.
  • Material Science: The compound is explored in the development of advanced materials, including polymers and nanomaterials, due to its ability to enhance material properties through chemical modification.

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