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Catalog Number:
38414
CAS Number:
206658-89-1
3-Aminophenylboronic acid monohydrate (contains varying amounts of anhydride)
Purity:
97 - 116% (Assay by Titration)
Synonym(s):
3-Aminobenzeneboronic acid monohydrate (contains varying amounts of anhydride)
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Product Information

3-Aminophenylboronic acid monohydrate is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique properties allow it to serve as a key building block in the synthesis of biologically active molecules, including inhibitors for proteases and other enzymes. Researchers appreciate its role in Suzuki-Miyaura cross-coupling reactions, which are fundamental in creating complex organic structures.

In addition to its applications in drug discovery, 3-Aminophenylboronic acid monohydrate is also employed in the development of sensors and materials for detecting glucose and other biomolecules, showcasing its relevance in the field of diagnostics. The compound's stability and ease of handling further enhance its appeal for both laboratory and industrial applications, making it a preferred choice for professionals seeking reliable and effective reagents in their work.

Synonyms
3-Aminobenzeneboronic acid monohydrate (contains varying amounts of anhydride)
CAS Number
206658-89-1
Purity
97 - 116% (Assay by Titration)
Molecular Formula
C6H8BNO2·H2O
Molecular Weight
154.97
MDL Number
MFCD00007755
PubChem ID
14389423
Melting Point
93 - 96 ?C
Appearance
White to almost white powder to crystal
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3-Aminobenzeneboronic acid monohydrate (contains varying amounts of anhydride)
CAS Number
206658-89-1
Purity
97 - 116% (Assay by Titration)
Molecular Formula
C6H8BNO2·H2O
Molecular Weight
154.97
MDL Number
MFCD00007755
PubChem ID
14389423
Melting Point
93 - 96 ?C
Appearance
White to almost white powder to crystal
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

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

  • Drug Development: This compound plays a crucial role in the synthesis of pharmaceuticals, particularly in developing anti-cancer agents. Its ability to form stable complexes with biomolecules enhances drug efficacy.
  • Bioconjugation: It is used in bioconjugation techniques to attach biomolecules to surfaces or other molecules, facilitating the development of targeted therapies and diagnostic tools in the biomedical field.
  • Organic Electronics: The compound is applied in the production of organic semiconductors, which are essential for developing flexible electronic devices, such as organic light-emitting diodes (OLEDs).
  • Material Science: It is utilized in creating advanced materials with specific properties, such as improved thermal stability and mechanical strength, beneficial in various industrial applications.
  • Chemical Sensing: The compound serves as a key component in chemical sensors, allowing for the detection of specific analytes in environmental monitoring and safety applications.

Citations