Same-day shipping on in-stock products. 99.6% on time delivery rate.

Catalog Number:
05029
CAS Number:
204322-78-1
Fmoc-(R,S-3-amino-N-1-carboxymethyl-2,3,4,5-tetrahydro-1H-[1]benzazepine-2-one
Purity:
≥ 99% (HPLC)
Documents
$93.14 /100MG
Pack Size Availability Price
Request Bulk Quote
Product Information

Fmoc-(R,S)-3-amino-N-1-carboxymethyl-2,3,4,5-tetrahydro-1H-[1]benzazepine-2-one is a versatile compound widely utilized in peptide synthesis and drug development. This compound features a unique Fmoc (fluorenylmethyloxycarbonyl) protecting group, which is essential for the selective protection of amino groups during the synthesis of peptides. Its structure allows for the incorporation of a benzazepine moiety, making it particularly valuable in the design of bioactive molecules and pharmaceuticals. Researchers appreciate its stability and ease of use in various coupling reactions, which enhances the efficiency of peptide synthesis.

In addition to its role in peptide chemistry, this compound has potential applications in medicinal chemistry, particularly in the development of novel therapeutic agents targeting neurological disorders. Its unique structural characteristics may contribute to the design of compounds with improved bioavailability and specificity. As a result, Fmoc-(R,S)-3-amino-N-1-carboxymethyl-2,3,4,5-tetrahydro-1H-[1]benzazepine-2-one stands out as a valuable tool for researchers and industry professionals aiming to innovate in drug discovery and development.

CAS Number
204322-78-1
Purity
≥ 99% (HPLC)
Molecular Formula
C27H24N2O5
Molecular Weight
456.5
MDL Number
MFCD00270209
PubChem ID
2756206
Melting Point
213 - 215 ?C
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
CAS Number
204322-78-1
Purity
≥ 99% (HPLC)
Molecular Formula
C27H24N2O5
Molecular Weight
456.5
MDL Number
MFCD00270209
PubChem ID
2756206
Melting Point
213 - 215 ?C
Appearance
White powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Fmoc-(R,S)-3-amino-N-1-carboxymethyl-2,3,4,5-tetrahydro-1H-[1]benzazepine-2-one is widely utilized in research focused on

  • Peptide Synthesis: This compound serves as a protective group in the synthesis of peptides, allowing for selective reactions that enhance yield and purity.
  • Drug Development: It plays a crucial role in the development of pharmaceutical compounds, particularly in creating targeted therapies for various diseases.
  • Bioconjugation: The chemical is used in bioconjugation processes, facilitating the attachment of biomolecules to drugs, which can improve efficacy and reduce side effects.
  • Research in Neuroscience: It is applied in studies related to neurotransmitter systems, helping researchers understand complex brain functions and develop neuroactive drugs.
  • Material Science: The compound is explored in the development of novel materials with unique properties, contributing to advancements in nanotechnology and polymer science.

Citations