Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
40155
CAS Number:
216019-28-2
3-Isopropylphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3-Isopropylbenzeneboronic acid
Documents
$152.33 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

3-Isopropylphenylboronic 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 develop advanced materials, pharmaceuticals, and agrochemicals. Its application in the synthesis of biologically active compounds highlights its significance in drug discovery and development, particularly in creating targeted therapies.

The compound's stability and reactivity provide notable advantages over similar boronic acids, allowing for more efficient coupling reactions and higher yields. Additionally, its role in the preparation of functionalized polymers and organic materials showcases its potential in material science. With its broad applicability across various fields, 3-Isopropylphenylboronic acid stands out as a crucial tool for chemists aiming to innovate and enhance their research outcomes.

Synonyms
3-Isopropylbenzeneboronic acid
CAS Number
216019-28-2
Purity
97 - 105% (Assay by titration)
Molecular Formula
C9H13BO2
Molecular Weight
164.01
MDL Number
MFCD01074634
PubChem ID
2773478
Melting Point
75-80°C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Isopropylbenzeneboronic acid
CAS Number
216019-28-2
Purity
97 - 105% (Assay by titration)
Molecular Formula
C9H13BO2
Molecular Weight
164.01
MDL Number
MFCD01074634
PubChem ID
2773478
Melting Point
75-80°C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Isopropylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex organic molecules efficiently. Its ability to form stable complexes with various substrates makes it invaluable in developing pharmaceuticals.
  • Drug Development: In medicinal chemistry, it is used to modify drug candidates, enhancing their efficacy and selectivity. The presence of the boronic acid group can improve the solubility and bioavailability of therapeutic agents.
  • Bioconjugation: The compound is employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules. This is particularly useful in creating targeted drug delivery systems and diagnostic tools.
  • Material Science: It plays a role in the development of advanced materials, such as polymers and hydrogels, which are used in various applications including drug delivery and tissue engineering due to their tunable properties.
  • Environmental Applications: The compound can be utilized in the detection and removal of pollutants, particularly in water treatment processes, by forming complexes with heavy metals and organic contaminants, thus aiding in environmental remediation efforts.

Citations