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Catalog Number:
39967
CAS Number:
180516-87-4
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid
Purity:
≥ 98% (GC)
Synonym(s):
2-(4-Carboxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 4-Carboxyphenylboronic acid pinacol ester
Documents
$43.87 /1G
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Product Information

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid is a specialized compound known for its unique boron-containing structure, which enhances its utility in various chemical applications. This compound serves as a versatile building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its ability to participate in cross-coupling reactions makes it invaluable for researchers looking to create complex molecular architectures. Additionally, its stability and solubility in organic solvents facilitate ease of handling and application in laboratory settings.

The compound's distinctive properties allow it to be employed in the synthesis of functionalized materials, including polymers and dyes, where precise control over molecular structure is essential. Its role in medicinal chemistry is particularly noteworthy, as it can be utilized in the design of novel therapeutic agents. With its favorable characteristics, 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid stands out as a preferred choice for professionals seeking reliable and effective solutions in their research and development projects.

Synonyms
2-(4-Carboxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 4-Carboxyphenylboronic acid pinacol ester
CAS Number
180516-87-4
Purity
≥ 98% (GC)
Molecular Formula
C13H17BO4
Molecular Weight
248.09
MDL Number
MFCD01863710
PubChem ID
2734621
Melting Point
228 - 232 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-(4-Carboxyphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 4-Carboxyphenylboronic acid pinacol ester
CAS Number
180516-87-4
Purity
≥ 98% (GC)
Molecular Formula
C13H17BO4
Molecular Weight
248.09
MDL Number
MFCD01863710
PubChem ID
2734621
Melting Point
228 - 232 ?C
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-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic synthesis, enabling the creation of complex molecules in pharmaceuticals and agrochemicals.
  • Drug Development: Its unique boron-containing structure enhances the solubility and stability of drug candidates, making it valuable in the formulation of new medications.
  • Polymer Chemistry: Used in the development of advanced materials, it contributes to the production of polymers with improved properties, such as thermal stability and mechanical strength.
  • Fluorescent Probes: The compound's ability to form stable complexes with metal ions makes it an excellent candidate for use in fluorescent probes in biological imaging applications.
  • Environmental Applications: It can be utilized in the design of sensors for detecting pollutants, aiding in environmental monitoring and protection efforts.

Citations