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Catalog Number:
40344
CAS Number:
154549-38-9
2,4,6-Triisopropylphenylboronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
2,4,6-Triisopropylbenzeneboronic acid
Documents
$68.20 /1G
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Product Information

2,4,6-Triisopropylphenylboronic acid is a versatile organoboron compound recognized for its significant role in organic synthesis and medicinal chemistry. This compound features a triisopropylphenyl group, which enhances its solubility and stability, making it an excellent choice for various applications. It is particularly useful in Suzuki-Miyaura coupling reactions, a fundamental method for forming carbon-carbon bonds, which is essential in the development of pharmaceuticals and agrochemicals. Additionally, its unique structure allows for selective binding in biological systems, making it a valuable tool in drug discovery and development.

Researchers and industry professionals appreciate 2,4,6-Triisopropylphenylboronic acid for its efficiency in facilitating complex organic transformations while minimizing by-products. Its robust nature and compatibility with various reaction conditions make it a preferred choice for those looking to streamline their synthetic pathways. With its potential to enhance reaction yields and simplify purification processes, this compound stands out in the field of synthetic organic chemistry.

Synonyms
2,4,6-Triisopropylbenzeneboronic acid
CAS Number
154549-38-9
Purity
≥ 98% (HPLC)
Molecular Formula
C15H25BO2
Molecular Weight
248.17
MDL Number
MFCD02683099
PubChem ID
15153544
Melting Point
165 °C (dec.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
2,4,6-Triisopropylbenzeneboronic acid
CAS Number
154549-38-9
Purity
≥ 98% (HPLC)
Molecular Formula
C15H25BO2
Molecular Weight
248.17
MDL Number
MFCD02683099
PubChem ID
15153544
Melting Point
165 °C (dec.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,4,6-Triisopropylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, facilitating the formation of complex molecules through Suzuki coupling reactions, which are essential for creating pharmaceuticals and agrochemicals.
  • Drug Development: In medicinal chemistry, it plays a crucial role in the design of boron-containing drugs, which can enhance the efficacy and selectivity of therapeutic agents, particularly in cancer treatment.
  • Material Science: It is used in the development of advanced materials, such as polymers and nanomaterials, where its unique properties can improve mechanical strength and thermal stability.
  • Bioconjugation: The compound is valuable in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is vital for diagnostics and targeted drug delivery systems.
  • Environmental Applications: It can be utilized in the detection and removal of pollutants, as its boronic acid functionality can selectively bind to certain environmental contaminants, aiding in water purification processes.

Citations