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Catalog Number:
22714
CAS Number:
946682-32-2
Ácido R , S -Fmoc-3-amino-3-( terc -butil)propiónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
( R , S -Fmoc-3-( terc -butil)-β-Ala-OH
Documents
$93.14 /100 mg
Tamaño
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Product Information

(R,S)-Fmoc-3-amino-3-(tert-butyl)propionic acid is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its unique structure, characterized by a tert-butyl side chain, enhances solubility and stability, making it an ideal choice for researchers in organic chemistry and biochemistry.

In practical applications, (R,S)-Fmoc-3-amino-3-(tert-butyl)propionic acid is employed in the synthesis of complex peptides and biologically active compounds, facilitating the development of pharmaceuticals and therapeutic agents. Its ability to provide steric hindrance while maintaining reactivity allows for greater control in synthetic pathways, leading to higher yields and purities. This compound is particularly beneficial in the fields of medicinal chemistry and biotechnology, where precision and efficiency are paramount.

Synonyms
( R , S -Fmoc-3-( terc -butil)-β-Ala-OH
CAS Number
946682-32-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C22H25NO4
Molecular Weight
367.44
MDL Number
MFCD09264210
PubChem ID
17040203
Melting Point
129-139 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
( R , S -Fmoc-3-( terc -butil)-β-Ala-OH
CAS Number
946682-32-2
Purity
≥ 98 % (HPLC)
Molecular Formula
C22H25NO4
Molecular Weight
367.44
MDL Number
MFCD09264210
PubChem ID
17040203
Melting Point
129-139 ?C
Appearance
Polvo blanco
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(R,S)-Fmoc-3-amino-3-(tert-butyl)propionic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing for the introduction of tert-butyl groups that enhance stability and solubility.
  • Drug Development: It plays a crucial role in the pharmaceutical industry for developing new drugs, particularly in creating compounds with improved bioavailability and efficacy.
  • Bioconjugation: Researchers use it for bioconjugation processes, linking biomolecules to create targeted therapies, which is essential in the field of personalized medicine.
  • Protein Engineering: The compound is employed in protein engineering to modify amino acid sequences, facilitating the design of proteins with specific functions or properties.
  • Research in Neuroscience: Its applications extend to neuroscience, where it aids in the development of neuroprotective agents, potentially leading to advancements in treating neurodegenerative diseases.

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