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Catalog Number:
07313
CAS Number:
214139-28-3
Acide Fmoc-( R , S -1-aminoindane-1-carboxylique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide Fmoc-DL-1-aminoindane-1-carboxylique
Documents
$100.05 /250 mg
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Product Information

Fmoc-(R,S)-1-aminoindane-1-carboxylic acid is a versatile compound widely utilized in the field of peptide synthesis and medicinal chemistry. This amino acid derivative features a fluorenylmethoxycarbonyl (Fmoc) protecting group, which is crucial for the selective protection of amino groups during the synthesis of peptides. Its unique structure allows for efficient incorporation into peptide chains, making it an essential building block for researchers developing novel therapeutics and bioactive compounds.

The compound's application extends to the synthesis of complex peptides that may exhibit enhanced biological activity, thereby facilitating advancements in drug discovery and development. Its ability to provide stability and solubility in various solvents enhances its utility in laboratory settings. Additionally, Fmoc-(R,S)-1-aminoindane-1-carboxylic acid stands out due to its potential for use in asymmetric synthesis, offering researchers a pathway to create enantiomerically pure compounds. This feature is particularly valuable in the pharmaceutical industry, where the chirality of compounds can significantly influence their efficacy and safety profiles.

Synonyms
Acide Fmoc-DL-1-aminoindane-1-carboxylique
CAS Number
214139-28-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 25 H 214
Molecular Weight
399.45
MDL Number
MFCD01321019
PubChem ID
2733196
Appearance
Poudre amorphe blanche
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Acide Fmoc-DL-1-aminoindane-1-carboxylique
CAS Number
214139-28-3
Purity
≥ 98 % (HPLC)
Molecular Formula
C 25 H 214
Molecular Weight
399.45
MDL Number
MFCD01321019
PubChem ID
2733196
Appearance
Poudre amorphe blanche
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-(R,S)-1-aminoindane-1-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions and improving yields in complex peptide chains.
  • Drug Development: Its unique structure makes it valuable in the design of new pharmaceuticals, particularly in creating compounds that target specific receptors in the body.
  • Bioconjugation: The chemical is used in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutic applications.
  • Research in Neuroscience: Its derivatives are explored in studies related to neurological pathways, potentially leading to advancements in treatments for mental health disorders.
  • Material Science: The compound's properties can be harnessed in the development of novel materials, such as polymers that exhibit unique mechanical or thermal characteristics.

Citations