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Catalog Number:
15071
CAS Number:
882847-29-2
Ácido 4-[2-(Fmoc-amino)etiloxi]benzoico
Purity:
≥ 99 % (HPLC)
Documents
$86.23 /100 mg
Tamaño
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Product Information

4-[2-(Fmoc-amino)ethyloxy]benzoic acid is a versatile compound widely utilized in the field of peptide synthesis and drug development. This compound features a unique Fmoc (fluorenylmethyloxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its structure allows for efficient coupling reactions, making it an invaluable tool for researchers aiming to create complex peptide sequences. The ethoxy group enhances solubility, facilitating smoother reactions and improving yields.

In practical applications, this compound is particularly beneficial in the pharmaceutical industry, where it is employed in the development of therapeutic peptides and biologically active compounds. Its ability to protect amino groups while allowing for subsequent modifications makes it a preferred choice for chemists working on drug design and synthesis. Additionally, its compatibility with various coupling reagents and conditions further underscores its utility in diverse synthetic pathways, making it a reliable option for both academic and industrial research.

CAS Number
882847-29-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 24 H 21 N º 5
Molecular Weight
403.43
MDL Number
MFCD04112692
PubChem ID
2756175
Melting Point
197-208 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
882847-29-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C 24 H 21 N º 5
Molecular Weight
403.43
MDL Number
MFCD04112692
PubChem ID
2756175
Melting Point
197-208 ?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

4-[2-(Fmoc-amino)ethyloxy]benzoic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the design of pharmaceutical compounds, particularly in optimizing drug delivery systems by enhancing solubility and stability.
  • Bioconjugation: The chemical is used to create bioconjugates, which are vital in developing targeted therapies and diagnostic tools in the biomedical field.
  • Material Science: It is involved in the formulation of advanced materials, such as polymers and nanomaterials, which have applications in electronics and coatings.
  • Research Reagents: This compound is a valuable reagent in various chemical reactions, aiding researchers in synthesizing complex molecules efficiently.

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