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Catalog Number:
12989
CAS Number:
157887-82-6
3-(Fmoc-amino)-1-propanol
Purity:
≥ 99 % (HPLC)
Synonym(s):
9-Fluorényl-méthyl N-(3-hydroxypropyl)carbamate
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Product Information

Élément constitutif pour la synthèse d'analogues et d'homologues oxa de polyamines naturelles

Synonyms
9-Fluorényl-méthyl N-(3-hydroxypropyl)carbamate
CAS Number
157887-82-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C 18 H 193
Molecular Weight
297.35
MDL Number
MFCD00409484
PubChem ID
2736488
Melting Point
127 - 128 °C
Appearance
Poudre blanche
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
9-Fluorényl-méthyl N-(3-hydroxypropyl)carbamate
CAS Number
157887-82-6
Purity
≥ 99 % (HPLC)
Molecular Formula
C 18 H 193
Molecular Weight
297.35
MDL Number
MFCD00409484
PubChem ID
2736488
Melting Point
127 - 128 °C
Appearance
Poudre blanche
Conditions
Conserver à 0 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-(Fmoc-amino)-1-propanol 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 structures for drug development and biological studies.
  • Drug Development: Its unique properties make it valuable in the pharmaceutical industry for developing new therapeutic agents, particularly those targeting specific biological pathways.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach drugs or imaging agents to biomolecules, enhancing their efficacy and specificity.
  • Research in Neuroscience: It plays a role in studying neurotransmitter systems, aiding in the development of treatments for neurological disorders.
  • Material Science: The compound is also explored in the development of new materials, particularly in creating functional polymers with specific properties for various applications.

Citations