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Catalog Number:
40371
CAS Number:
147621-18-9
6-Indoleboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
6-Indolylboronic acid
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Product Information

6-Indoleboronic acid is a versatile compound widely recognized for its applications in medicinal chemistry and organic synthesis. This boronic acid derivative features a unique indole structure, which enhances its reactivity and selectivity in various chemical reactions. Its ability to form stable complexes with diols makes it particularly valuable in the development of sensors and probes for biological applications. Researchers utilize 6-Indoleboronic acid in the synthesis of pharmaceuticals, especially in the design of anti-cancer agents and other therapeutic compounds. Furthermore, its role as a building block in the preparation of complex organic molecules underscores its importance in both academic research and industrial applications.

The compound's distinctive properties, such as its moderate solubility in water and compatibility with a range of solvents, make it an ideal candidate for diverse chemical reactions. Its applications extend to the fields of materials science and catalysis, where it can be employed in the development of novel materials and catalytic systems. By integrating 6-Indoleboronic acid into your research or production processes, you can leverage its unique characteristics to enhance the efficiency and effectiveness of your chemical endeavors.

Synonyms
6-Indolylboronic acid
CAS Number
147621-18-9
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H8BNO2
Molecular Weight
160.97
MDL Number
MFCD03095176
PubChem ID
2763205
Melting Point
200 °C (dec.)
Appearance
White to light orange to green powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
6-Indolylboronic acid
CAS Number
147621-18-9
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H8BNO2
Molecular Weight
160.97
MDL Number
MFCD03095176
PubChem ID
2763205
Melting Point
200 °C (dec.)
Appearance
White to light orange to green powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

6-Indoleboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key building block in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents due to its ability to interact with biological targets.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the specificity and efficacy of drug delivery systems.
  • Fluorescent Probes: The compound is used to create fluorescent probes for biological imaging, helping scientists visualize cellular processes in real-time, which is crucial for understanding disease mechanisms.
  • Organic Electronics: In the field of organic electronics, it is utilized in the fabrication of organic semiconductors, contributing to the development of flexible and efficient electronic devices.
  • Catalysis: This chemical acts as a catalyst in various organic reactions, improving reaction rates and selectivity, which is beneficial for chemists looking to optimize synthetic pathways.

Citations