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Catalog Number:
40337
CAS Number:
246023-54-1
Ácido 4-metoxi-2,5-dimetilfenilborónico
Purity:
98 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 4-metoxi-2,5-dimetilbencenoborónico
Documents
$115.27 /1G
Tamaño
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Product Information

4-Methoxy-2,5-dimethylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure, featuring a methoxy group and two methyl substituents, enhances its reactivity and selectivity, allowing for the efficient formation of carbon-carbon bonds. Researchers appreciate its role in developing novel compounds with potential therapeutic applications, particularly in the field of cancer research and drug discovery.

In addition to its synthetic utility, 4-Methoxy-2,5-dimethylphenylboronic acid exhibits favorable solubility characteristics, which facilitate its use in various reaction conditions. Its compatibility with a range of functional groups makes it an attractive choice for chemists looking to streamline their synthetic pathways. With its proven efficacy in diverse applications, this compound stands out as a valuable resource for professionals seeking to innovate in organic synthesis and medicinal chemistry.

Synonyms
Ácido 4-metoxi-2,5-dimetilbencenoborónico
CAS Number
246023-54-1
Purity
98 - 105% (Ensayo por titulación)
Molecular Formula
C 9 H 13 BO 3
Molecular Weight
180.01
MDL Number
MFCD06801676
PubChem ID
5233015
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 4-metoxi-2,5-dimetilbencenoborónico
CAS Number
246023-54-1
Purity
98 - 105% (Ensayo por titulación)
Molecular Formula
C 9 H 13 BO 3
Molecular Weight
180.01
MDL Number
MFCD06801676
PubChem ID
5233015
Appearance
Polvo cristalino de color blanco a blanquecino.
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

4-Methoxy-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.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura cross-coupling reactions, allowing researchers to create complex carbon-carbon bonds efficiently, which is essential in drug discovery.
  • Bioconjugation: The boronic acid functionality enables selective binding to diols, making it useful in bioconjugation processes for labeling biomolecules in diagnostics and therapeutic applications.
  • Material Science: This compound is applied in the development of advanced materials, including polymers and nanomaterials, enhancing properties such as conductivity and mechanical strength.
  • Sensor Development: Its ability to interact with specific biomolecules makes it valuable in creating sensors for detecting glucose and other metabolites, beneficial in medical diagnostics.

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