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Catalog Number:
40272
CAS Number:
123291-97-4
2-Ethoxy-5-methylphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
2-Ethoxy-5-methylbenzeneboronic acid
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Product Information

2-Ethoxy-5-methylphenylboronic acid is a versatile boronic acid derivative known for its significant role in organic synthesis and medicinal chemistry. This compound features a unique structure that allows it to participate in various cross-coupling reactions, making it an essential reagent for the formation of carbon-carbon bonds. Its ability to selectively bind to diols enhances its utility in the development of complex organic molecules, particularly in the synthesis of pharmaceuticals and agrochemicals. Researchers appreciate its effectiveness in Suzuki-Miyaura coupling reactions, where it facilitates the formation of aryl-aryl bonds, crucial for creating diverse chemical libraries.

In addition to its synthetic applications, 2-Ethoxy-5-methylphenylboronic acid is recognized for its potential in the development of targeted therapies, particularly in cancer research. Its boron atom can interact with biological molecules, opening avenues for innovative drug design. The compound's stability and ease of handling make it a preferred choice for both academic and industrial laboratories. With its broad applicability and unique properties, 2-Ethoxy-5-methylphenylboronic acid stands out as a valuable tool for chemists seeking to advance their research and development projects.

Synonyms
2-Ethoxy-5-methylbenzeneboronic acid
CAS Number
123291-97-4
Purity
95 - 105% (Assay by titration)
Molecular Formula
C9H13BO3
Molecular Weight
180.01
MDL Number
MFCD00196832
PubChem ID
4615191
Melting Point
94 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-Ethoxy-5-methylbenzeneboronic acid
CAS Number
123291-97-4
Purity
95 - 105% (Assay by titration)
Molecular Formula
C9H13BO3
Molecular Weight
180.01
MDL Number
MFCD00196832
PubChem ID
4615191
Melting Point
94 °C (Lit.)
Appearance
White to off-white 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-Ethoxy-5-methylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura coupling reactions, allowing chemists to form carbon-carbon bonds efficiently, which is essential in creating various organic compounds.
  • Drug Development: The compound is significant in medicinal chemistry for designing and optimizing drug candidates, particularly in targeting specific biological pathways.
  • Material Science: It is used in the development of advanced materials, including polymers and nanomaterials, enhancing properties such as conductivity and strength.
  • Bioconjugation: This chemical facilitates the attachment of biomolecules to surfaces or other molecules, which is vital in creating biosensors and targeted drug delivery systems.

Citations