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Catalog Number:
40199
CAS Number:
338454-30-1
4-Benzyloxy-3-methylphenylboronic acid
Purity:
96 - 105% (Assay by titration)
Synonym(s):
4-Benzyloxy-3-methylbenzeneboronic acid
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Product Information

4-Benzyloxy-3-methylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valuable 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 facilitate the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its selective reactivity and compatibility with various functional groups enhance its utility in developing innovative compounds with specific biological activities.

In addition to its role in synthetic chemistry, 4-Benzyloxy-3-methylphenylboronic acid is also explored for applications in materials science, particularly in the development of boron-containing polymers and materials with tailored properties. Its ability to act as a building block for more complex structures opens avenues for research in drug discovery and development, where precision and efficiency are paramount. This compound stands out for its ease of use and effectiveness in various applications, making it a preferred choice for chemists seeking reliable and efficient reagents.

Synonyms
4-Benzyloxy-3-methylbenzeneboronic acid
CAS Number
338454-30-1
Purity
96 - 105% (Assay by titration)
Molecular Formula
C14H15BO3
Molecular Weight
242.08
MDL Number
MFCD06409944
PubChem ID
17750522
Melting Point
130 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Benzyloxy-3-methylbenzeneboronic acid
CAS Number
338454-30-1
Purity
96 - 105% (Assay by titration)
Molecular Formula
C14H15BO3
Molecular Weight
242.08
MDL Number
MFCD06409944
PubChem ID
17750522
Melting Point
130 °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

4-Benzyloxy-3-methylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: It plays a crucial role in the design of boron-containing drugs, which can enhance the efficacy of treatments for diseases such as cancer and diabetes.
  • Cross-Coupling Reactions: This chemical is essential in Suzuki-Miyaura cross-coupling reactions, allowing researchers to create complex molecular structures efficiently.
  • Bioconjugation: It is used in bioconjugation processes to attach biomolecules to surfaces or other molecules, which is vital in developing targeted drug delivery systems.
  • Analytical Chemistry: The compound can be employed in sensor development for detecting specific biomolecules, aiding in diagnostics and environmental monitoring.

Citations