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Catalog Number:
40190
CAS Number:
55499-44-0
Ácido 2,4-dimetilfenilborónico
Purity:
95 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 2,4-dimetilbencenoborónico, Ácido m -xileno-4-borónico
Documents
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Product Information

2,4-Dimethylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. Known for its ability to form stable complexes with various substrates, this boronic acid derivative is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are essential for the formation of carbon-carbon bonds. Its unique structure allows for selective reactivity, making it an ideal choice for researchers aiming to develop complex organic molecules, including pharmaceuticals and agrochemicals.

Additionally, 2,4-Dimethylphenylboronic acid serves as a key intermediate in the synthesis of biologically active compounds, enhancing its relevance in drug discovery and development. Its compatibility with diverse functional groups and ease of handling further contribute to its appeal in laboratory settings. Whether you are working on advanced materials or exploring new therapeutic agents, this compound offers significant advantages in efficiency and effectiveness compared to other boronic acids, making it a preferred choice for professionals in the field.

Synonyms
Ácido 2,4-dimetilbencenoborónico, Ácido m -xileno-4-borónico
CAS Number
55499-44-0
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C8H11BO2
Molecular Weight
149.98
MDL Number
MFCD02683101
PubChem ID
4198739
Melting Point
192 - 195 °C
Appearance
Polvo cristalino de color blanco a amarillo claro.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 2,4-dimetilbencenoborónico, Ácido m -xileno-4-borónico
CAS Number
55499-44-0
Purity
95 - 105% (Ensayo por titulación)
Molecular Formula
C8H11BO2
Molecular Weight
149.98
MDL Number
MFCD02683101
PubChem ID
4198739
Melting Point
192 - 195 °C
Appearance
Polvo cristalino de color blanco a amarillo claro.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,4-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 essential in Suzuki-Miyaura coupling reactions, allowing researchers to create complex carbon-carbon bonds efficiently, which is crucial in materials science and drug development.
  • Sensor Development: The compound is used in the fabrication of sensors for detecting sugars and other biomolecules, making it valuable in the fields of biochemistry and medical diagnostics.
  • Polymer Chemistry: It acts as a modifier in the production of boron-containing polymers, enhancing their properties for applications in electronics and coatings.
  • Research in Catalysis: Its unique boronic acid functionality makes it a useful ligand in catalytic processes, improving reaction selectivity and efficiency in various chemical transformations.

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