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Catalog Number:
11569
CAS Number:
77716-11-1
4-(Boc-amino)-1-methyl-1H-pyrrole-2-carboxylic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Boc-Py-OH
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Product Information

4-(Boc-amino)-1-methyl-1H-pyrrole-2-carboxylic acid is a versatile compound widely utilized in the field of organic synthesis and medicinal chemistry. This compound features a Boc (tert-butyloxycarbonyl) protecting group, which enhances its stability and reactivity, making it an excellent choice for peptide synthesis and other complex organic reactions. Its unique structure allows for the introduction of various functional groups, facilitating the development of novel pharmaceuticals and biologically active molecules. Researchers appreciate its role in the synthesis of pyrrole derivatives, which are crucial in the design of drugs targeting a range of diseases, including cancer and neurological disorders.

In addition to its applications in drug development, 4-(Boc-amino)-1-methyl-1H-pyrrole-2-carboxylic acid serves as a valuable intermediate in the production of agrochemicals and fine chemicals. Its ability to undergo various transformations while maintaining structural integrity makes it a preferred choice for chemists seeking to optimize reaction conditions and improve yields. This compound not only streamlines synthetic pathways but also enhances the efficiency of research and development processes in both academic and industrial settings.

Synonyms
Boc-Py-OH
CAS Number
77716-11-1
Purity
≥ 99% (HPLC)
Molecular Formula
C11H16N2O4
Molecular Weight
240.26
MDL Number
MFCD02094544
PubChem ID
2735636
Appearance
White to pale yellow powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Boc-Py-OH
CAS Number
77716-11-1
Purity
≥ 99% (HPLC)
Molecular Formula
C11H16N2O4
Molecular Weight
240.26
MDL Number
MFCD02094544
PubChem ID
2735636
Appearance
White to pale yellow 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-(Boc-amino)-1-methyl-1H-pyrrole-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, allowing researchers to create complex molecules for pharmaceutical applications.
  • Drug Development: It plays a significant role in the development of new drugs, particularly in the design of compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Bioconjugation: The compound is used in bioconjugation processes, where it helps attach drugs to biomolecules, improving drug delivery systems and targeting capabilities.
  • Research in Neuroscience: Its unique structure makes it valuable in neuroscience research, particularly in studying neuroactive compounds and their interactions in the brain.
  • Material Science: The compound is also explored in material science for creating novel polymers and materials with specific properties, such as increased stability and functionality.

Citations