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Catalog Number:
15050
CAS Number:
141636-66-0
Fmoc-(S)-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
Fmoc-D-Dtc-OH
Documents
$134.70 /250MG
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Product Information

Fmoc-(S)-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique thiazolidine core, which enhances its stability and reactivity, making it an excellent choice for researchers focused on developing novel peptides and bioactive compounds. Its Fmoc (fluorenylmethyloxycarbonyl) protecting group allows for easy deprotection under mild conditions, facilitating streamlined synthesis processes.

In the pharmaceutical industry, this compound is particularly valuable for the development of peptide-based drugs, where its structural properties can lead to improved bioavailability and efficacy. Additionally, its application in combinatorial chemistry opens avenues for high-throughput screening of potential therapeutic candidates. With its robust profile, Fmoc-(S)-5,5-dimethyl-1,3-thiazolidine-4-carboxylic acid stands out as a crucial reagent for researchers aiming to innovate in drug discovery and development.

Synonyms
Fmoc-D-Dtc-OH
CAS Number
141636-66-0
Purity
≥ 98% (HPLC)
Molecular Formula
C21H21NO4S
Molecular Weight
383.46
MDL Number
MFCD02682321
PubChem ID
4712563
Appearance
White powder
Optical Rotation
[a]D25 = +50 ± 2 º (C=1 in DMF)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-D-Dtc-OH
CAS Number
141636-66-0
Purity
≥ 98% (HPLC)
Molecular Formula
C21H21NO4S
Molecular Weight
383.46
MDL Number
MFCD02682321
PubChem ID
4712563
Appearance
White powder
Optical Rotation
[a]D25 = +50 ± 2 º (C=1 in DMF)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(S)-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 the synthesis of peptides, allowing for selective reactions without interfering with other functional groups.
  • Drug Development: It is used in the design of novel pharmaceuticals, particularly in the creation of compounds that target specific biological pathways.
  • Bioconjugation: The chemical is valuable in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Research in Organic Chemistry: It aids researchers in exploring new synthetic routes and methodologies, contributing to advancements in organic synthesis techniques.
  • Analytical Chemistry: This compound is employed in various analytical applications, including chromatography, to help separate and identify complex mixtures.

Citations