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Catalog Number:
29705
CAS Number:
1310680-20-6
Ácido R , S -Fmoc-3,3-dimetil-pirrolidin-2-carboxílico
Purity:
≥ 99 % (HPLC)
Synonym(s):
( R , S -Fmoc-3,3-dimetil-prolina
Documents
$86.23 /25 mg
Tamaño
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Product Information

(R,S)-Fmoc-3,3-dimethyl-pyrrolidine-2-carboxylic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound, known for its protective Fmoc (9-fluorenylmethyloxycarbonyl) group, facilitates the selective modification of amino acids, making it an essential tool for researchers in the fields of medicinal chemistry and biochemistry. Its unique structure enhances stability and solubility, allowing for efficient coupling reactions in solid-phase peptide synthesis.

This compound is particularly valuable in the synthesis of complex peptides and peptidomimetics, which are crucial for developing therapeutic agents. Its ability to provide steric hindrance while maintaining reactivity makes it an attractive choice for chemists looking to optimize their synthetic pathways. With applications ranging from drug discovery to the production of biologically active compounds, (R,S)-Fmoc-3,3-dimethyl-pyrrolidine-2-carboxylic acid stands out as a reliable and effective reagent for advancing research and development in pharmaceutical sciences.

Synonyms
( R , S -Fmoc-3,3-dimetil-prolina
CAS Number
1310680-20-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H23NO4
Molecular Weight
365.43
MDL Number
MFCD18782844
PubChem ID
74788892
Melting Point
123-134 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
( R , S -Fmoc-3,3-dimetil-prolina
CAS Number
1310680-20-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C22H23NO4
Molecular Weight
365.43
MDL Number
MFCD18782844
PubChem ID
74788892
Melting Point
123-134 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R,S)-Fmoc-3,3-dimethyl-pyrrolidine-2-carboxylic acid is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protective group in peptide synthesis, allowing for the selective modification of amino acids. Its stability under various reaction conditions makes it a preferred choice for researchers developing complex peptides.
  • Drug Development: In pharmaceutical research, it is used to create bioactive peptides that can lead to new therapeutic agents. Its ability to enhance solubility and bioavailability is particularly beneficial in drug formulation.
  • Bioconjugation: The compound is employed in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, facilitating the development of targeted drug delivery systems.
  • Material Science: It finds applications in the creation of functional materials, such as hydrogels, which can be used in tissue engineering and regenerative medicine due to its biocompatibility.
  • Analytical Chemistry: Researchers utilize this compound in analytical methods for the detection and quantification of various biomolecules, enhancing the sensitivity and accuracy of assays.

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