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Catalog Number:
40339
CAS Number:
357611-51-9
3,5-Dimethyl-4-propoxyphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3,5-Dimethyl-4-propoxybenzeneboronic acid
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Product Information

3,5-Dimethyl-4-propoxyphenylboronic 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 enhances its reactivity, making it an excellent candidate for Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds. Its ability to selectively bind to diols allows for applications in the development of sensors and drug delivery systems, particularly in targeting specific biomolecules. Researchers appreciate its stability and compatibility with various reaction conditions, which facilitates its use in complex synthetic pathways.

In the pharmaceutical industry, 3,5-Dimethyl-4-propoxyphenylboronic acid is utilized in the synthesis of biologically active compounds, contributing to the development of new therapeutic agents. Its properties make it particularly valuable in the design of inhibitors and other compounds that require precise molecular interactions. With its growing importance in research and development, this boronic acid derivative stands out for its practical applications and potential to drive innovation in chemical synthesis and drug discovery.

Synonyms
3,5-Dimethyl-4-propoxybenzeneboronic acid
CAS Number
357611-51-9
Purity
97 - 105% (Assay by titration)
Molecular Formula
C11H17BO3
Molecular Weight
208.06
MDL Number
MFCD05865178
PubChem ID
16217512
Melting Point
187 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3,5-Dimethyl-4-propoxybenzeneboronic acid
CAS Number
357611-51-9
Purity
97 - 105% (Assay by titration)
Molecular Formula
C11H17BO3
Molecular Weight
208.06
MDL Number
MFCD05865178
PubChem ID
16217512
Melting Point
187 °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

3,5-Dimethyl-4-propoxyphenylboronic 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.
  • Drug Development: It is employed in medicinal chemistry for the design and synthesis of boron-containing drugs, which can enhance the efficacy of treatments for various diseases, including cancer.
  • Bioconjugation: The compound is used in bioconjugation processes, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial in developing targeted therapies and diagnostics.
  • Sensor Technology: Its unique properties make it suitable for creating sensors that detect specific biomolecules, aiding in medical diagnostics and environmental monitoring.
  • Material Science: This boronic acid derivative is utilized in the development of advanced materials, including polymers and nanomaterials, which have applications in electronics and energy storage.

Citations