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Catalog Number:
30523
CAS Number:
873842-06-9
Ácido 4R -Fmoc-2,2-dimetil-1,3-tiazolidina-4-carboxílico
Purity:
98,5 - 100,0% (Ensayo por titulación)
Synonym(s):
Fmoc-L-Thz(Me2)-OH, Fmoc-2,2-dimetil-L-tiaprolina
Antibiotic
Documents
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Product Information

(4R)-3-Fmoc-2,2-dimethyl-1,3-thiazolidine-4-carboxylic acid is a versatile compound widely utilized in peptide synthesis and drug development. Its unique structure, featuring a fluorenylmethoxycarbonyl (Fmoc) protecting group, allows for efficient protection of amino acids during the synthesis of complex peptides. This compound is particularly valuable in the field of medicinal chemistry, where it aids in the design and production of bioactive peptides, enhancing the efficacy of therapeutic agents. Researchers appreciate its stability and compatibility with various coupling reagents, making it an ideal choice for solid-phase peptide synthesis.

In addition to its role in peptide synthesis, (4R)-3-Fmoc-2,2-dimethyl-1,3-thiazolidine-4-carboxylic acid is also explored for its potential applications in drug formulation and delivery systems. Its favorable properties enable the development of novel therapeutic compounds with improved bioavailability and targeted delivery. This compound stands out for its ability to streamline the synthesis process while maintaining high purity and yield, making it a preferred choice for professionals in pharmaceutical and biotechnological research.

Synonyms
Fmoc-L-Thz(Me2)-OH, Fmoc-2,2-dimetil-L-tiaprolina
CAS Number
873842-06-9
Purity
98,5 - 100,0% (Ensayo por titulación)
Molecular Formula
C21H21NO4S
Molecular Weight
383.5
MDL Number
MFCD05665145
PubChem ID
75627318
Melting Point
148 - 160 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = -18 a -23 º (C=1 en DMF)
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Fmoc-L-Thz(Me2)-OH, Fmoc-2,2-dimetil-L-tiaprolina
CAS Number
873842-06-9
Purity
98,5 - 100,0% (Ensayo por titulación)
Molecular Formula
C21H21NO4S
Molecular Weight
383.5
MDL Number
MFCD05665145
PubChem ID
75627318
Melting Point
148 - 160 ?C
Appearance
Polvo cristalino blanco
Optical Rotation
[a] D 20 = -18 a -23 º (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

(4R)-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 protective group in the synthesis of peptides, allowing for selective reactions and improving yield in complex organic synthesis.
  • Drug Development: It is used in the design of pharmaceutical compounds, particularly in the development of new drugs targeting specific biological pathways, enhancing the efficacy of therapeutic agents.
  • Bioconjugation: The compound facilitates the attachment of biomolecules to surfaces or other molecules, which is crucial in creating targeted drug delivery systems and improving the specificity of treatments.
  • Research in Medicinal Chemistry: It plays a role in the exploration of thiazolidine derivatives, which have shown potential in treating various diseases, including metabolic disorders.
  • Analytical Chemistry: This compound is utilized in the development of analytical methods for detecting and quantifying specific biomolecules, aiding in quality control and research applications.

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