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Catalog Number:
16181
CAS Number:
915714-21-5
(S-Nα-Fmoc-Nβ-Boc-2,3-diaminopropan-1-ol
Purity:
≥ 99% (HPLC)
Synonym(s):
Fmoc-L-Dap(Boc)-ol, (S-2-(Fmoc-amino)-3-(Boc-amino)-1-propanol
Documents
$70.00 /100MG
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Product Information

(S)-Na-Fmoc-Nb-Boc-2,3-diaminopropan-1-ol is a versatile compound widely utilized in peptide synthesis and medicinal chemistry. This compound features a unique combination of protective groups, including the Fmoc (9-fluorenylmethyloxycarbonyl) and Boc (tert-butoxycarbonyl) moieties, which facilitate selective reactions and enhance the stability of the amine functionalities during synthesis. Its chiral nature allows for the production of enantiomerically pure compounds, making it invaluable in the development of pharmaceuticals and biologically active molecules.

Researchers and industry professionals can leverage (S)-Na-Fmoc-Nb-Boc-2,3-diaminopropan-1-ol for the efficient synthesis of complex peptides and other bioactive compounds. Its ability to protect amino groups while allowing for further functionalization makes it an essential tool in drug discovery and development. Additionally, its favorable solubility and compatibility with various reaction conditions enhance its utility in diverse applications, from academic research to large-scale pharmaceutical production.

Synonyms
Fmoc-L-Dap(Boc)-ol, (S-2-(Fmoc-amino)-3-(Boc-amino)-1-propanol
CAS Number
915714-21-5
Purity
≥ 99% (HPLC)
Molecular Formula
C23H28N2O5
Molecular Weight
412.5
MDL Number
MFCD04973190
PubChem ID
75627353
Melting Point
149-159 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -6 ± 0.5º (C=1 in MeOH)
Conditions
Store at 0-8 °C
General Information
Synonyms
Fmoc-L-Dap(Boc)-ol, (S-2-(Fmoc-amino)-3-(Boc-amino)-1-propanol
CAS Number
915714-21-5
Purity
≥ 99% (HPLC)
Molecular Formula
C23H28N2O5
Molecular Weight
412.5
MDL Number
MFCD04973190
PubChem ID
75627353
Melting Point
149-159 °C
Appearance
White crystalline powder
Optical Rotation
[a]D20 = -6 ± 0.5º (C=1 in MeOH)
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(S)-Na-Fmoc-Nb-Boc-2,3-diaminopropan-1-ol 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 and biological studies.
  • Drug Development: Its unique structure enhances the solubility and stability of pharmaceutical compounds, making it valuable in the formulation of new medications.
  • Bioconjugation: The chemical is used in bioconjugation processes, linking biomolecules to enhance their functionality, which is crucial in developing targeted therapies.
  • Research in Neuroscience: It plays a role in the synthesis of compounds that can modulate neurotransmitter activity, aiding in the study of neurological disorders.
  • Material Science: The compound can be incorporated into polymers to improve their properties, such as flexibility and strength, benefiting various industrial applications.

Citations