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Catalog Number:
40094
CAS Number:
90002-36-1
2-Ethylphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
2-Ethylbenzeneboronic acid
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Product Information

2-Ethylphenylboronic acid is a versatile organoboron compound widely utilized in organic synthesis and medicinal chemistry. This compound is particularly valued for its ability to form stable complexes with various substrates, making it an essential reagent in cross-coupling reactions, such as Suzuki-Miyaura coupling. Its unique structure allows for enhanced reactivity and selectivity, which is crucial for the development of complex organic molecules, including pharmaceuticals and agrochemicals. Researchers appreciate its role in the synthesis of biologically active compounds, where precision and efficiency are paramount.

In addition to its applications in synthetic chemistry, 2-Ethylphenylboronic acid is also employed in the development of sensors and materials due to its boron functionality. Its ability to interact with diols and other nucleophiles opens avenues for creating innovative materials with tailored properties. This compound stands out for its compatibility with various reaction conditions, making it a reliable choice for both academic and industrial applications. With its broad range of uses, 2-Ethylphenylboronic acid is an invaluable tool for chemists seeking to push the boundaries of organic synthesis and material science.

Synonyms
2-Ethylbenzeneboronic acid
CAS Number
90002-36-1
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H11BO2
Molecular Weight
149.98
MDL Number
MFCD02093075
PubChem ID
4100862
Melting Point
108 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-Ethylbenzeneboronic acid
CAS Number
90002-36-1
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H11BO2
Molecular Weight
149.98
MDL Number
MFCD02093075
PubChem ID
4100862
Melting Point
108 °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-Ethylphenylboronic 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, enhancing the efficiency of chemical reactions.
  • Drug Development: It plays a crucial role in medicinal chemistry, especially in the design of boron-containing drugs that target specific biological pathways, offering potential therapeutic benefits in treating diseases.
  • Chemical Sensors: The compound is employed in the creation of chemical sensors for detecting biomolecules, such as glucose, which can be vital for diabetes management and monitoring.
  • Polymer Chemistry: It is used in the modification of polymers, improving their properties for applications in coatings, adhesives, and materials science, leading to enhanced performance and durability.
  • Bioconjugation: This chemical is advantageous in bioconjugation processes, allowing for the attachment of biomolecules to surfaces or other compounds, which is essential in the development of targeted drug delivery systems.

Citations