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Catalog Number:
15057
CAS Number:
195387-29-2
4-(Fmoc-amino)-1-methylpyrrole-2-carboxylic acid
Purity:
≥ 97% (HPLC)
Synonym(s):
Fmoc-Py-OH
Documents
$85.60 /100MG
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Product Information

4-(Fmoc-amino)-1-methylpyrrole-2-carboxylic acid is a versatile building block widely utilized in peptide synthesis and medicinal chemistry. This compound features a protective Fmoc (9-fluorenylmethoxycarbonyl) group, which allows for selective deprotection during the synthesis of complex peptides, making it invaluable for researchers in the field of drug development. Its unique structure, combining a pyrrole ring with a carboxylic acid functionality, enhances its reactivity and compatibility with various coupling reactions, facilitating the creation of diverse peptide sequences.

In addition to its role in peptide synthesis, this compound is also explored for its potential applications in the development of novel pharmaceuticals, particularly in targeting specific biological pathways. Researchers appreciate its stability and ease of handling, which contribute to efficient experimental workflows. With its ability to streamline the synthesis of bioactive compounds, 4-(Fmoc-amino)-1-methylpyrrole-2-carboxylic acid stands out as a crucial tool for chemists aiming to innovate in drug discovery and development.

Synonyms
Fmoc-Py-OH
CAS Number
195387-29-2
Purity
≥ 97% (HPLC)
Molecular Formula
C21H18N2O4
Molecular Weight
362.38
MDL Number
MFCD02094546
PubChem ID
2756159
Melting Point
196 - 210 °C
Appearance
White powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Fmoc-Py-OH
CAS Number
195387-29-2
Purity
≥ 97% (HPLC)
Molecular Formula
C21H18N2O4
Molecular Weight
362.38
MDL Number
MFCD02094546
PubChem ID
2756159
Melting Point
196 - 210 °C
Appearance
White powder
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

4-(Fmoc-amino)-1-methylpyrrole-2-carboxylic acid is widely utilized in research focused on:

  • Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in solid-phase peptide synthesis, enhancing the efficiency and yield of desired products.
  • Drug Development: It plays a significant role in the pharmaceutical industry for the development of novel drugs, especially those targeting specific biological pathways, due to its ability to modify amino acids.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, facilitating the study of protein interactions and functions.
  • Research in Neuroscience: It is applied in neuroscience research to create compounds that can cross the blood-brain barrier, making it valuable for studying neurological disorders and developing treatments.
  • Material Science: This chemical is utilized in the development of advanced materials, including polymers and coatings, due to its unique chemical properties that enhance material performance.

Citations