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Catalog Number:
15051
CAS Number:
753030-79-4
Fmoc-R)-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-Dtc-OH
Documents
$113.87 /250MG
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Product Information

Fmoc-(R)-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique thiazolidine ring structure, which enhances its stability and reactivity, making it an ideal choice for researchers focused on developing novel therapeutic agents. Its Fmoc (9-fluorenylmethyloxycarbonyl) protecting group allows for easy incorporation into peptide chains, facilitating the synthesis of complex peptides with high purity and yield.

In the pharmaceutical industry, this compound has shown potential in the design of bioactive peptides, particularly in applications related to drug delivery systems and targeted therapies. Its ability to form stable conjugates with various biomolecules opens avenues for innovative research in medicinal chemistry. Researchers appreciate its ease of use and compatibility with standard coupling reagents, which streamlines the synthesis process. Overall, Fmoc-(R)-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid stands out for its practical applications in advancing peptide-based therapeutics.

Synonyms
Fmoc-L-Dtc-OH
CAS Number
753030-79-4
Purity
≥ 99% (HPLC)
Molecular Formula
C21H21NO4S
Molecular Weight
383.46
MDL Number
MFCD02682349
PubChem ID
4712563
Melting Point
68-76 ºC
Optical Rotation
[a]=49 ± 2 º (C=1 in DMF)
Conditions
Store at 0-8°C
General Information
Synonyms
Fmoc-L-Dtc-OH
CAS Number
753030-79-4
Purity
≥ 99% (HPLC)
Molecular Formula
C21H21NO4S
Molecular Weight
383.46
MDL Number
MFCD02682349
PubChem ID
4712563
Melting Point
68-76 ºC
Optical Rotation
[a]=49 ± 2 º (C=1 in DMF)
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(R)-5,5-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 for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It is used in the design of novel pharmaceuticals, particularly in the development of compounds that target specific biological pathways, enhancing drug efficacy.
  • Bioconjugation: The compound facilitates the attachment of biomolecules, such as proteins or nucleic acids, to other molecules, which is crucial in creating targeted therapies and diagnostics.
  • Research in Organic Chemistry: Its unique structure allows chemists to explore new synthetic routes and methodologies, contributing to advancements in organic synthesis techniques.
  • Material Science: The compound is also explored in the development of new materials, particularly in creating polymers with specific properties for industrial applications.

Citations