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

Catalog Number:
22680
CAS Number:
182624-46-0
2 S ,11a S -Fmoc-2-amino-10-carboxyméthyl-1,2,3,11a-tétrahydro-10H-pyrrolo[2,1- c ][1,4]-benzodiazépine-5,11-dione
Purity:
≥ 99 % (HPLC)
Synonym(s):
Fmoc-PBD
Documents
$99.85 /25 mg
Taille
Request Bulk Quote
Product Information

The compound (2S,11aS)-Fmoc-2-amino-10-carboxymethyl-1,2,3,11a-tetrahydro-10H-pyrrolo[2,1-c][1,4]-benzodiazepine is a versatile building block in peptide synthesis and drug development. Known for its unique structure, this compound features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is widely utilized in solid-phase peptide synthesis. Its ability to stabilize peptide chains while allowing for selective deprotection makes it an invaluable tool for researchers in medicinal chemistry and biochemistry.

This compound is particularly beneficial in the design of bioactive peptides, enabling the development of therapeutics with enhanced efficacy and specificity. Its structural attributes facilitate the synthesis of complex molecules, making it ideal for applications in pharmaceutical research, particularly in the fields of oncology and neurology. The compound's stability and reactivity profile also provide advantages over similar compounds, ensuring higher yields and purity in synthetic processes.

Synonyms
Fmoc-PBD
CAS Number
182624-46-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C29H25N3O6
Molecular Weight
511.53
MDL Number
MFCD06656486
PubChem ID
4712615
Appearance
Poudre blanche
Optical Rotation
[a] D 20
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Fmoc-PBD
CAS Number
182624-46-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C29H25N3O6
Molecular Weight
511.53
MDL Number
MFCD06656486
PubChem ID
4712615
Appearance
Poudre blanche
Optical Rotation
[a] D 20
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

(2S,11aS)-Fmoc-2-amino-10-carboxymethyl-1,2,3,11a-tetrahydro-10H-pyrrolo[2,1-c][1,4]-benzodiazepine 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 affecting the overall structure.
  • Drug Development: Its unique structure makes it a valuable building block in the design of novel pharmaceuticals, particularly in the development of compounds targeting neurological disorders.
  • Bioconjugation: The chemical can be used in bioconjugation processes, facilitating the attachment of biomolecules to therapeutic agents, enhancing their efficacy and specificity.
  • Research in Neuroscience: It is utilized in studies related to neurotransmitter systems, aiding researchers in understanding complex brain functions and developing potential treatments.
  • Analytical Chemistry: The compound is beneficial in analytical applications, including chromatography, where it helps in the separation and identification of complex mixtures.

Citations