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Catalog Number:
40079
CAS Number:
216485-86-8
3-Isopropoxyphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
3-Isopropoxybenzeneboronic acid
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Product Information

3-Isopropoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized 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 application extends to the development of sensors and catalysts, where its boron functionality enhances reactivity and selectivity in various chemical transformations.

The compound's stability and reactivity make it particularly advantageous compared to other boronic acids, allowing for more efficient reactions under mild conditions. Its role in the synthesis of biologically active compounds underscores its significance in drug discovery and development. With its growing importance in the field of materials science and nanotechnology, 3-Isopropoxyphenylboronic acid stands out as a valuable tool for researchers aiming to innovate and enhance their chemical processes.

Synonyms
3-Isopropoxybenzeneboronic acid
CAS Number
216485-86-8
Purity
95 - 105% (Assay by titration)
Molecular Formula
C9H13BO3
Molecular Weight
180.01
MDL Number
MFCD03701512
PubChem ID
5083932
Melting Point
81 °C (Lit.)
Density
1.07 g/mL
Appearance
White to light yellow crystalline powder
Boiling Point
199 °C (Lit.)
Conditions
Store at RT
General Information
Synonyms
3-Isopropoxybenzeneboronic acid
CAS Number
216485-86-8
Purity
95 - 105% (Assay by titration)
Molecular Formula
C9H13BO3
Molecular Weight
180.01
MDL Number
MFCD03701512
PubChem ID
5083932
Melting Point
81 °C (Lit.)
Density
1.07 g/mL
Appearance
White to light yellow crystalline powder
Boiling Point
199 °C (Lit.)
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-Isopropoxyphenylboronic 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.
  • Medicinal Chemistry: It is employed in drug discovery processes, especially for creating boron-containing compounds that can enhance the efficacy of certain medications.
  • Bioconjugation: The unique properties of this boronic acid make it suitable for bioconjugation applications, allowing researchers to attach biomolecules to surfaces or other compounds for targeted delivery.
  • Sensor Development: It is used in the fabrication of chemical sensors, particularly for detecting glucose levels, which is crucial for diabetes management.
  • Material Science: This compound is incorporated into polymer materials to improve their mechanical properties and thermal stability, making it valuable in various industrial applications.

Citations