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Catalog Number:
22752
CAS Number:
1076197-00-6
Acide Fmoc-3-amino-2,2-diméthyl-propionique
Purity:
≥ 98 % (HPLC)
Documents
$80.50 /100 mg
Taille
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Product Information

Fmoc-3-amino-2,2-dimethyl-propionic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound, known for its protective Fmoc (9-fluorenylmethyloxycarbonyl) group, allows for selective deprotection, making it an essential tool for chemists in the field of organic synthesis. Its unique structure not only enhances solubility but also provides stability during the synthesis process, which is crucial for producing high-purity peptides. Researchers appreciate its application in solid-phase peptide synthesis (SPPS), where it facilitates the assembly of complex peptide sequences with precision and efficiency.

Additionally, Fmoc-3-amino-2,2-dimethyl-propionic acid serves as a valuable intermediate in the development of pharmaceuticals and biologically active compounds. Its ability to introduce sterically hindered amino acids into peptide chains opens avenues for creating novel therapeutics with improved bioactivity and selectivity. This compound is particularly relevant for those working in medicinal chemistry and biochemistry, as it supports the design of peptides with enhanced properties for targeted drug delivery and therapeutic applications.

CAS Number
1076197-00-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C 20 H 214
Molecular Weight
339.39
MDL Number
MFCD09952626
PubChem ID
45024431
Appearance
Solide vitreux blanc ou solide pelucheux
Conditions
Conserver à 0 - 8 °C
General Information
CAS Number
1076197-00-6
Purity
≥ 98 % (HPLC)
Molecular Formula
C 20 H 214
Molecular Weight
339.39
MDL Number
MFCD09952626
PubChem ID
45024431
Appearance
Solide vitreux blanc ou solide pelucheux
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

Fmoc-3-amino-2,2-dimethyl-propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in solid-phase peptide synthesis, allowing for the selective modification of amino acids without interfering with other functional groups.
  • Drug Development: It plays a crucial role in the design of peptide-based therapeutics, particularly in enhancing the stability and bioavailability of drug candidates.
  • Bioconjugation: The compound is effective in bioconjugation processes, facilitating the attachment of peptides to various biomolecules, which is essential in creating targeted drug delivery systems.
  • Research in Neuroscience: Its derivatives are often used in studies related to neurotransmitter systems, helping researchers understand the role of peptides in neurological functions.
  • Protein Engineering: This chemical aids in the development of modified proteins with enhanced properties, making it valuable in biotechnology applications.

Citations