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Catalog Number:
18999
CAS Number:
885273-97-2
Acide 2-(4- N -Fmoc-morpholin-2-yl)acétique
Purity:
≥ 95 % (HPLC)
Synonym(s):
4-Fmoc-2-carboxyméthyl-morpholine
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$173.66 /100 mg
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Product Information

2-(4-N-Fmoc-morpholin-2-yl)acetic acid is a versatile compound widely utilized in the field of peptide synthesis and drug development. This compound features a morpholine ring, which enhances its solubility and stability, making it an excellent choice for researchers looking to develop complex peptide structures. Its unique N-Fmoc (9H-fluoren-9-ylmethoxycarbonyl) protecting group allows for selective deprotection, facilitating the synthesis of peptides with high purity and yield. This characteristic is particularly beneficial in the pharmaceutical industry, where precision and efficiency are paramount.

In addition to its applications in peptide synthesis, 2-(4-N-Fmoc-morpholin-2-yl)acetic acid serves as a valuable building block in the development of various bioactive compounds. Its ability to form stable linkages with other functional groups opens up possibilities for creating novel therapeutics. Researchers can leverage this compound in medicinal chemistry to explore new avenues for drug discovery, particularly in targeting specific biological pathways. With its favorable properties and broad applicability, this compound is an essential tool for professionals in the fields of chemistry and pharmaceuticals.

Synonyms
4-Fmoc-2-carboxyméthyl-morpholine
CAS Number
885273-97-2
Purity
≥ 95 % (HPLC)
Molecular Formula
C 21 H 215
Molecular Weight
367.4
MDL Number
MFCD00270203
PubChem ID
65814710
Appearance
Cire jaune
Conditions
Conserver à 0-8 °C
General Information
Synonyms
4-Fmoc-2-carboxyméthyl-morpholine
CAS Number
885273-97-2
Purity
≥ 95 % (HPLC)
Molecular Formula
C 21 H 215
Molecular Weight
367.4
MDL Number
MFCD00270203
PubChem ID
65814710
Appearance
Cire jaune
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

2-(4-N-Fmoc-morpholin-2-yl)acetic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, 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 enhancing the solubility and stability of drug candidates.
  • Bioconjugation: The chemical is used in bioconjugation techniques, enabling the attachment of biomolecules to surfaces or other molecules, which is essential in developing targeted therapies.
  • Research on Enzyme Inhibitors: It is employed in studies aimed at discovering new enzyme inhibitors, contributing to advancements in treatments for various diseases.
  • Analytical Chemistry: The compound is utilized in analytical methods for detecting and quantifying biomolecules, aiding in quality control and research applications.

Citations