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Catalog Number:
40141
CAS Number:
66472-86-4
3-Aminophenylboronic acid Hemisulfate
Purity:
95 - 105% (Assay by titration)
Synonym(s):
3-Aminobenzeneboronic acid hemisulfate
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Product Information

3-Aminophenylboronic acid Hemisulfate is a versatile compound widely utilized in the fields of organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique structure not only enhances its reactivity but also allows for the development of various pharmaceuticals, particularly in the synthesis of biologically active compounds. Researchers appreciate its role in the preparation of targeted drug candidates, especially in oncology and neurobiology, where precision in molecular design is crucial.

Additionally, 3-Aminophenylboronic acid Hemisulfate serves as a valuable tool in the development of sensors and diagnostic assays due to its affinity for specific biomolecules. Its application in the creation of boron-based fluorescent probes highlights its potential in bioimaging and tracking cellular processes. With its combination of reactivity and specificity, this compound stands out as a key player in advancing research and development across multiple scientific disciplines.

Synonyms
3-Aminobenzeneboronic acid hemisulfate
CAS Number
66472-86-4
Purity
95 - 105% (Assay by titration)
Molecular Formula
C6H8BNO2·0.5H2SO4
Molecular Weight
185.98
MDL Number
MFCD00013111
PubChem ID
16211139
Melting Point
> 300 °C
Appearance
White to amber to dark green crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Aminobenzeneboronic acid hemisulfate
CAS Number
66472-86-4
Purity
95 - 105% (Assay by titration)
Molecular Formula
C6H8BNO2·0.5H2SO4
Molecular Weight
185.98
MDL Number
MFCD00013111
PubChem ID
16211139
Melting Point
> 300 °C
Appearance
White to amber to dark green crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Aminophenylboronic acid Hemisulfate is widely utilized in research focused on:

  • Drug Development: This compound plays a crucial role in the synthesis of boron-containing pharmaceuticals, which can enhance the efficacy of certain drugs by improving their bioavailability.
  • Bioconjugation: It is used in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other compounds, facilitating the development of targeted therapies and diagnostics.
  • Organic Synthesis: The compound serves as a versatile building block in organic synthesis, enabling the creation of complex molecules with applications in materials science and nanotechnology.
  • Sensor Development: Its unique properties make it ideal for developing sensors that detect specific biomolecules, which is valuable in medical diagnostics and environmental monitoring.
  • Research in Catalysis: The compound is utilized in catalytic processes, offering advantages in reaction efficiency and selectivity compared to traditional catalysts, thus benefiting various chemical industries.

Citations