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Catalog Number:
30522
Ácido 4 S -3-Fmoc-2,2-dimetil-1,3-tiazolidina-4-carboxílico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-Thz(Me2)-OH, Fmoc-2,2-dimetil-D-tiaprolina
Antibiotic
Documents
$72.31 /250 mg
Tamaño
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Product Information

The compound (4S)-3-Fmoc-2,2-dimethyl-1,3-thiazolidine-4-carboxylic acid is a valuable building block in peptide synthesis and medicinal chemistry. This thiazolidine derivative is particularly notable for its role in the development of peptide-based pharmaceuticals, where it serves as a protecting group for amino acids. Its unique structure enhances the stability and solubility of peptides, making it an essential component in the synthesis of complex biomolecules. Researchers appreciate its ability to facilitate the formation of peptide bonds while providing a straightforward means of deprotection, which is crucial in the final stages of peptide synthesis.

In addition to its applications in peptide synthesis, this compound has shown potential in drug discovery and development, particularly in the design of inhibitors and modulators for various biological targets. Its favorable properties, including high stability and compatibility with various reaction conditions, make it an attractive choice for chemists looking to streamline their synthetic processes. With its proven utility in both academic and industrial settings, (4S)-3-Fmoc-2,2-dimethyl-1,3-thiazolidine-4-carboxylic acid stands out as a versatile tool for advancing research and development in the pharmaceutical sector.

Synonyms
Fmoc-D-Thz(Me2)-OH, Fmoc-2,2-dimetil-D-tiaprolina
Purity
≥ 99 % (HPLC)
Molecular Formula
C21H21NO4S
Molecular Weight
383.5
MDL Number
MFCD06858314
Melting Point
155-160 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = +21 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-D-Thz(Me2)-OH, Fmoc-2,2-dimetil-D-tiaprolina
Purity
≥ 99 % (HPLC)
Molecular Formula
C21H21NO4S
Molecular Weight
383.5
MDL Number
MFCD06858314
Melting Point
155-160 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = +21 ± 2º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
DEA-regulated
No
Warnings
-
Applications

(4S)-3-Fmoc-2,2-dimethyl-1,3-thiazolidine-4-carboxylic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protecting group in peptide synthesis, allowing chemists to selectively modify amino acids without affecting others. This is crucial for creating complex peptides used in drug development.
  • Drug Development: Its unique structure aids in the design of new pharmaceuticals, particularly in creating compounds that can interact effectively with biological targets, enhancing drug efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, linking biomolecules to drugs or imaging agents, which is essential in targeted therapy and diagnostics in medicine.
  • Research in Organic Chemistry: It provides a versatile framework for exploring new reactions and mechanisms, helping researchers develop innovative synthetic pathways and methodologies.
  • Material Science: The compound can be incorporated into polymers or materials, enhancing their properties for applications in coatings, adhesives, and other advanced materials.

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