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Catalog Number:
40254
CAS Number:
85199-06-0
2,5-Dimethylphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
2,5-Dimethylbenzeneboronic acid, p-Xylene-2-boronic acid
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Product Information

2,5-Dimethylphenylboronic 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 Suzuki-Miyaura cross-coupling reactions. Its unique structure allows for selective functionalization, which is crucial in the development of pharmaceuticals and agrochemicals. Researchers have effectively employed 2,5-Dimethylphenylboronic acid in the synthesis of various biologically active compounds, showcasing its potential in drug discovery and development.

In addition to its role in organic synthesis, 2,5-Dimethylphenylboronic acid is also recognized for its applications in sensor technology and materials science. Its ability to interact with carbohydrates and other biomolecules opens avenues for the development of biosensors and diagnostic tools. The compound's stability and reactivity make it an attractive choice for researchers looking to innovate in these fields. With its broad range of applications and benefits, 2,5-Dimethylphenylboronic acid stands out as a valuable tool for professionals in chemistry and related industries.

Synonyms
2,5-Dimethylbenzeneboronic acid, p-Xylene-2-boronic acid
CAS Number
85199-06-0
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H11BO2
Molecular Weight
149.98
MDL Number
MFCD01863525
PubChem ID
2734347
Melting Point
192 °C (Lit.)
Appearance
White to slightly yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
2,5-Dimethylbenzeneboronic acid, p-Xylene-2-boronic acid
CAS Number
85199-06-0
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H11BO2
Molecular Weight
149.98
MDL Number
MFCD01863525
PubChem ID
2734347
Melting Point
192 °C (Lit.)
Appearance
White to slightly yellow 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

2,5-Dimethylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals, enhancing the efficiency of chemical reactions.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in complex organic compounds, making it valuable in the production of fine chemicals.
  • Sensor Development: The compound is used in the fabrication of sensors for detecting biomolecules, offering high sensitivity and selectivity, which is beneficial in medical diagnostics and environmental monitoring.
  • Material Science: It contributes to the development of advanced materials, including polymers and nanomaterials, which are used in electronics and coatings, providing improved performance and durability.
  • Biological Applications: This boronic acid derivative is explored for its potential in drug delivery systems and as a therapeutic agent, particularly in targeting specific biological pathways, thus presenting a promising avenue in medicinal chemistry.

Citations