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Catalog Number:
18477
CAS Number:
317830-84-5
Éster de pinacol del ácido 1-( terc -butoxicarbonil)-1 H -indol-5-ilborónico
Purity:
≥ 99% (GC)
Synonym(s):
Éster de pinacol del ácido 1-Boc-indol-5-borónico
Documents
$146.92 /1G
Tamaño
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Product Information

1-(tert-Butoxycarbonyl)-1H-indol-5-ylboronic acid pinacol ester is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to participate in cross-coupling reactions, making it an essential building block in the development of complex organic molecules. Its unique structure allows for the selective functionalization of indole derivatives, which are crucial in the synthesis of pharmaceuticals and agrochemicals. Researchers appreciate its stability and ease of handling, which facilitate its incorporation into various synthetic pathways.

In addition to its synthetic applications, this compound has shown promise in the development of targeted therapies due to its ability to form reversible covalent bonds with biomolecules. This property enhances its potential in drug discovery, particularly in designing inhibitors for specific enzymes. The compound's compatibility with diverse reaction conditions further broadens its applicability in both academic and industrial settings, making it a valuable asset for chemists seeking efficient and effective solutions in their research and development projects.

Synonyms
Éster de pinacol del ácido 1-Boc-indol-5-borónico
CAS Number
317830-84-5
Purity
≥ 99% (GC)
Molecular Formula
C13H16BNO4
Molecular Weight
261.08
MDL Number
MFCD05663895
PubChem ID
18375637
Appearance
Marrón claro sólido
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Éster de pinacol del ácido 1-Boc-indol-5-borónico
CAS Number
317830-84-5
Purity
≥ 99% (GC)
Molecular Formula
C13H16BNO4
Molecular Weight
261.08
MDL Number
MFCD05663895
PubChem ID
18375637
Appearance
Marrón claro sólido
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1-(tert-Butoxycarbonyl)-1H-indol-5-ylboronic acid pinacol ester is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of novel anti-cancer agents.
  • Organic Synthesis: It is employed in cross-coupling reactions, allowing chemists to create complex organic molecules efficiently, which is essential in materials science and drug discovery.
  • Bioconjugation: The compound can be used in bioconjugation processes, facilitating the attachment of drugs to biomolecules, enhancing targeted delivery in therapeutic applications.
  • Research in Catalysis: It plays a role in catalysis research, particularly in the development of new catalytic systems that can improve reaction efficiency and selectivity.
  • Analytical Chemistry: This chemical is utilized in the development of analytical methods for detecting and quantifying other compounds, providing valuable tools for quality control in various industries.

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