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Catalog Number:
17419
CAS Number:
352359-23-0
Ácido 1-Boc-5-fluoro-1 H -indol-2-borónico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ácido 5-fluoro-1- tert -butoxicarbonilindol-2-borónico, Ácido N- (Boc)-5-fluoroindol-2-borónico
Documents
$72.31 /250 mg
Tamaño
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Product Information

1-Boc-5-fluoro-1H-indole-2-boronic acid is a versatile compound that plays a significant role in pharmaceutical research and development. This boronic acid derivative is particularly valuable in the synthesis of biologically active molecules, especially in the field of medicinal chemistry. Its unique structure, featuring a boronic acid functional group, allows for efficient coupling reactions, making it an essential building block in the creation of complex organic compounds. Researchers utilize this compound in the development of targeted therapies, particularly in oncology, where it can aid in the design of inhibitors that selectively target cancer cells.

The presence of the Boc (tert-butyloxycarbonyl) protecting group enhances the stability and solubility of the compound, facilitating its use in various synthetic pathways. Additionally, the fluorine atom in its structure can influence the compound's biological activity and pharmacokinetic properties, making it a subject of interest for drug discovery. With its potential applications in synthesizing novel therapeutic agents and its advantageous properties, 1-Boc-5-fluoro-1H-indole-2-boronic acid is an invaluable resource for researchers and industry professionals seeking to innovate in the pharmaceutical landscape.

Synonyms
Ácido 5-fluoro-1- tert -butoxicarbonilindol-2-borónico, Ácido N- (Boc)-5-fluoroindol-2-borónico
CAS Number
352359-23-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 13 H 15 BF N º 4
Molecular Weight
279.07
MDL Number
MFCD04114581
PubChem ID
2763292
Melting Point
116-122 ?C
Appearance
Sólido blanco
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido 5-fluoro-1- tert -butoxicarbonilindol-2-borónico, Ácido N- (Boc)-5-fluoroindol-2-borónico
CAS Number
352359-23-0
Purity
≥ 99 % (HPLC)
Molecular Formula
C 13 H 15 BF N º 4
Molecular Weight
279.07
MDL Number
MFCD04114581
PubChem ID
2763292
Melting Point
116-122 ?C
Appearance
Sólido blanco
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-Boc-5-fluoro-1H-indole-2-boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial intermediate in the synthesis of various pharmaceuticals, particularly in developing targeted cancer therapies due to its ability to inhibit specific enzymes.
  • Bioconjugation: It is used in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other compounds, enhancing drug delivery systems and improving therapeutic efficacy.
  • Material Science: The compound is applied in creating advanced materials, including polymers and nanomaterials, which can be utilized in electronics and coatings, offering improved performance and durability.
  • Fluorescent Probes: It acts as a building block for fluorescent probes, aiding in biological imaging and diagnostics, which are essential for visualizing cellular processes in real-time.
  • Organic Synthesis: This chemical is a valuable reagent in organic synthesis, providing researchers with a versatile tool for constructing complex molecular architectures, thus streamlining the development of new compounds.

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