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Catalog Number:
40231
CAS Number:
55499-43-9
Acide 3,4-diméthylphénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 3,4-diméthylbenzèneboronique
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Product Information

3,4-Dimethylphenylboronic acid is a versatile compound widely utilized in 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. Researchers and industry professionals leverage its unique properties to develop pharmaceuticals, agrochemicals, and advanced materials. Its application in the synthesis of biologically active compounds highlights its significance in drug discovery and development.

Additionally, 3,4-Dimethylphenylboronic acid serves as a valuable tool in the field of sensor technology, particularly in the detection of glucose and other biomolecules. Its compatibility with various substrates enhances its utility in creating selective sensors. The compound's ease of handling and stability under standard laboratory conditions further contribute to its appeal, making it a preferred choice for researchers seeking reliable and efficient reagents for their projects.

Synonyms
Acide 3,4-diméthylbenzèneboronique
CAS Number
55499-43-9
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 11 BO 2
Molecular Weight
149.98
MDL Number
MFCD01009694
PubChem ID
2734348
Melting Point
220°C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide 3,4-diméthylbenzèneboronique
CAS Number
55499-43-9
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C 8 H 11 BO 2
Molecular Weight
149.98
MDL Number
MFCD01009694
PubChem ID
2734348
Melting Point
220°C (lit.)
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3,4-Dimethylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, facilitating the formation of carbon-carbon bonds, which is essential in creating complex organic structures.
  • Sensor Development: The compound can be employed in the design of chemical sensors for detecting carbohydrates and other biomolecules, enhancing the accuracy of biochemical assays.
  • Drug Discovery: Researchers leverage its properties to explore new drug candidates, particularly in targeting specific biological pathways, making it valuable in medicinal chemistry.
  • Material Science: It finds applications in the development of advanced materials, such as polymers and nanomaterials, which can be used in electronics and coatings.

Citations