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Catalog Number:
19649
CAS Number:
467442-21-3
Acide ( S )-2-(9H-fluorén-9-ylméthoxycarbonyl-amino)-4,4-difluoro-butyrique
Purity:
≥ 99 % (dosage)
Documents
$121.78 /25 mg
Taille
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Product Information

(S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4,4-difluoro-butyric acid is a specialized compound known for its unique structural properties and applications in the field of medicinal chemistry. This compound features a difluorobutanoic acid backbone, which enhances its biological activity, making it a valuable intermediate in the synthesis of pharmaceuticals. Its fluorenylmethoxycarbonyl (Fmoc) protecting group is particularly advantageous for peptide synthesis, allowing for the selective modification of amino acids while maintaining stability during various chemical reactions.

Researchers and industry professionals utilize this compound in the development of novel therapeutic agents, especially in the design of peptide-based drugs. Its ability to facilitate the introduction of fluorine atoms into molecular structures can lead to improved pharmacokinetic properties, such as increased metabolic stability and bioavailability. This compound's unique characteristics make it an essential tool for those looking to innovate in drug development and synthetic chemistry.

CAS Number
467442-21-3
Purity
≥ 99 % (dosage)
Molecular Formula
C 19 H 17 F 2 NON 4
Molecular Weight
361.34
MDL Number
MFCD06796145
PubChem ID
21063801
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0 - 8 °C
General Information
CAS Number
467442-21-3
Purity
≥ 99 % (dosage)
Molecular Formula
C 19 H 17 F 2 NON 4
Molecular Weight
361.34
MDL Number
MFCD06796145
PubChem ID
21063801
Appearance
Solide blanc à blanc cassé
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4,4-difluoro-butyric acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, enhancing the efficiency and selectivity of reactions.
  • Drug Development: It plays a crucial role in the design of new pharmaceuticals, particularly in optimizing the properties of drug candidates through structural modifications.
  • Biochemical Research: Researchers use it to study protein interactions and functions, providing insights into cellular mechanisms and potential therapeutic targets.
  • Material Science: The compound is applied in developing advanced materials, including polymers that require specific functional groups for enhanced performance.
  • Fluorine Chemistry: Its unique fluorinated structure allows for the exploration of fluorine's effects in various chemical reactions, leading to innovative applications in medicinal chemistry.

Citations