Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
04314
CAS Number:
134098-70-7
Ester α- tert -butylique de l'acide Fmoc-D-aspartique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-D-Asp-OtBu
Documents
93 /100
8 Citations
Bioz Stars Product Rating
The world's only objective ratings for scientific research products
Mentions 
Recency 
View product citations >
$93.14 /250 mg
Taille
Request Bulk Quote
Product Information

Fmoc-D-aspartic acid a-tert-butyl ester is a versatile building block widely utilized in peptide synthesis and drug development. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which allows for selective deprotection during the synthesis process, making it an ideal choice for researchers working on complex peptide sequences. Its tert-butyl ester group enhances solubility and stability, facilitating smoother reactions and improving yields in various organic synthesis applications.

This compound is particularly valuable in the fields of medicinal chemistry and biochemistry, where it serves as a precursor for the synthesis of bioactive peptides and pharmaceuticals. Researchers appreciate its ability to streamline the synthesis of peptides with specific functionalities, enabling the development of targeted therapies and novel drug candidates. With its unique properties, Fmoc-D-aspartic acid a-tert-butyl ester stands out as a crucial reagent for advancing peptide chemistry and enhancing the efficiency of drug discovery processes.

Synonyms
Fmoc-D-Asp-OtBu
CAS Number
134098-70-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C 23 H 256
Molecular Weight
411.5
MDL Number
MFCD00237011
PubChem ID
14702620
Melting Point
103-109 ºC
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = +24 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-D-Asp-OtBu
CAS Number
134098-70-7
Purity
≥ 99 % (HPLC)
Molecular Formula
C 23 H 256
Molecular Weight
411.5
MDL Number
MFCD00237011
PubChem ID
14702620
Melting Point
103-109 ºC
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = +24 ± 2º (C = 1 dans DMF)
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-D-aspartic acid a-tert-butyl ester is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for the selective modification of amino acids without affecting others. Its stability under various conditions makes it a preferred choice in the field.
  • Drug Development: In pharmaceutical research, it plays a crucial role in the design of peptide-based drugs, particularly those targeting neurological disorders, by providing a stable structure that can be easily modified.
  • Bioconjugation: This chemical is used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, enhancing the functionality of diagnostic tools and therapeutic agents.
  • Research in Neuroscience: It is instrumental in studying neurotransmitter systems, as its derivatives can mimic natural neurotransmitters, aiding in the development of treatments for conditions like depression and anxiety.
  • Material Science: The compound is also explored in the creation of smart materials, where its properties can be utilized to develop responsive systems for drug delivery or biosensing applications.