Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
40283
CAS Number:
22237-12-3
3-Amino-4-methylphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3-Amino-4-methylbenzeneboronic acid, 3-Amino-p-tolylboronic acid
Documents
$76.51 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

3-Amino-4-methylphenylboronic acid 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 enable it to act as a key building block in the synthesis of biologically active molecules, including those targeting cancer and other diseases. Researchers appreciate its role in Suzuki coupling reactions, which facilitate the formation of carbon-carbon bonds, thereby expanding the toolkit available for complex molecule construction.

In addition to its applications in drug discovery, 3-Amino-4-methylphenylboronic acid is also employed in the development of sensors and materials science, where its boronic acid functionality can be exploited for selective binding and detection of sugars and other biomolecules. This compound stands out due to its ease of handling and compatibility with various reaction conditions, making it a preferred choice for both academic and industrial laboratories. Its potential for innovation in diverse fields underscores its significance in advancing chemical research and development.

Synonyms
3-Amino-4-methylbenzeneboronic acid, 3-Amino-p-tolylboronic acid
CAS Number
22237-12-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H10BNO2
Molecular Weight
150.97
MDL Number
MFCD01074640
PubChem ID
2737803
Melting Point
250°C (Lit.)
Appearance
Light brown solid
Conditions
Store at 2 - 8 °C
General Information
Synonyms
3-Amino-4-methylbenzeneboronic acid, 3-Amino-p-tolylboronic acid
CAS Number
22237-12-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H10BNO2
Molecular Weight
150.97
MDL Number
MFCD01074640
PubChem ID
2737803
Melting Point
250°C (Lit.)
Appearance
Light brown solid
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Amino-4-methylphenylboronic 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 developing targeted therapies for cancer and other diseases.
  • Bioconjugation: Its boronic acid functionality allows for the selective binding to diols, making it valuable in creating bioconjugates for drug delivery systems and diagnostic applications.
  • Organic Electronics: It is used in the fabrication of organic semiconductors, contributing to the development of efficient electronic devices, such as organic light-emitting diodes (OLEDs).
  • Material Science: The compound is utilized in creating advanced materials with specific properties, such as enhanced thermal stability and mechanical strength, beneficial for various industrial applications.
  • Analytical Chemistry: It plays a role in the development of sensors and assays for detecting biomolecules, providing a reliable method for monitoring biological processes.

Citations