🌟 99% Happy customers

📦 Same-day shipping on in-stock items

Catalog Number:
05033
CAS Number:
204326-07-8, 149563-21-3
Acide Fmoc-(3 S ,6 S ,9 R )-2-oxo-3-amino-7-thia-1-azabicyclo[4.3.0]nonane-9-carboxylique
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-Btd-OH
Documents
$134.70 /25 mg
Taille
Request Bulk Quote
Product Information

Fmoc-(3S,6S,9R)-2-oxo-3-amino-7-thia-1-azabicyclo[4.3.0]nonane-9-carboxylic acid is a specialized compound widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique bicyclic structure that enhances its stability and reactivity, making it an ideal choice for researchers focused on developing novel peptides and therapeutic agents. Its Fmoc (9-fluorenylmethoxycarbonyl) protecting group allows for selective deprotection under mild conditions, facilitating the synthesis of complex peptide sequences.

In addition to its application in peptide synthesis, this compound has potential uses in drug discovery and development, particularly in the design of inhibitors and modulators for various biological targets. Its structural attributes contribute to improved binding affinity and specificity, making it a valuable tool for medicinal chemists. Researchers can leverage the unique properties of Fmoc-(3S,6S,9R)-2-oxo-3-amino-7-thia-1-azabicyclo[4.3.0]nonane-9-carboxylic acid to explore innovative therapeutic pathways and enhance the efficacy of their compounds.

Synonyms
Fmoc-Btd-OH
CAS Number
204326-07-8, 149563-21-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C23H22N2O5S
Molecular Weight
438.5
MDL Number
MFCD06797451
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -152 ± 2º (C = 1 dans DMF)
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-Btd-OH
CAS Number
204326-07-8, 149563-21-3
Purity
≥ 99 % (HPLC)
Molecular Formula
C23H22N2O5S
Molecular Weight
438.5
MDL Number
MFCD06797451
Appearance
Poudre blanche
Optical Rotation
[a] D 20 = -152 ± 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-(3S,6S,9R)-2-oxo-3-amino-7-thia-1-azabicyclo[4.3.0]nonane-9-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, allowing researchers to create complex molecules for drug development.
  • Pharmaceutical Development: It is used in the design of novel pharmaceuticals, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The chemical is employed in bioconjugation techniques, enabling the attachment of biomolecules to drugs or imaging agents, which improves targeting and reduces side effects.
  • Research in Neuroscience: It plays a role in studying neuroactive compounds, aiding in the development of treatments for neurological disorders by mimicking natural neurotransmitters.
  • Material Science: The compound is also explored in material science for developing smart materials that respond to environmental changes, showcasing its versatility beyond traditional applications.

Citations