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Catalog Number:
40056
CAS Number:
269409-73-6
Acide 3-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzoïque
Purity:
≥ 98% (CG)
Synonym(s):
2-(3-carboxyphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester pinacol de l'acide 3-carboxyphénylboronique
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Product Information

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid is a versatile compound known for its unique boron-containing structure, which enhances its reactivity and stability in various applications. This compound is particularly valuable in organic synthesis, serving as a key intermediate in the development of pharmaceuticals and agrochemicals. Its ability to participate in cross-coupling reactions makes it an essential building block for creating complex molecular architectures. Researchers appreciate its role in facilitating the formation of carbon-carbon bonds, which is crucial in the synthesis of biologically active compounds.

In addition to its synthetic utility, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid exhibits excellent solubility in organic solvents, making it suitable for a wide range of laboratory applications. Its stability under various conditions allows for prolonged use in reactions without significant degradation. This compound is ideal for researchers looking to streamline their synthesis processes while achieving high yields and purity. With its unique properties and practical applications, this compound stands out as a valuable asset in both academic and industrial settings.

Synonyms
2-(3-carboxyphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester pinacol de l'acide 3-carboxyphénylboronique
CAS Number
269409-73-6
Purity
≥ 98% (CG)
Molecular Formula
C 13 H 17 BO 4
Molecular Weight
248.09
MDL Number
MFCD03411930
PubChem ID
2734653
Melting Point
208 - 212 °C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
2-(3-carboxyphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, Ester pinacol de l'acide 3-carboxyphénylboronique
CAS Number
269409-73-6
Purity
≥ 98% (CG)
Molecular Formula
C 13 H 17 BO 4
Molecular Weight
248.09
MDL Number
MFCD03411930
PubChem ID
2734653
Melting Point
208 - 212 °C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-(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 the synthesis of various organic molecules, allowing chemists to create complex structures efficiently.
  • Drug Development: It plays a crucial role in medicinal chemistry, particularly in the design of new pharmaceuticals, by acting as a key intermediate in the synthesis of bioactive compounds.
  • Material Science: The compound is used in the development of advanced materials, including polymers and coatings, due to its unique chemical properties that enhance material performance.
  • Fluorescent Probes: It is utilized in creating fluorescent probes for biological imaging, enabling researchers to visualize cellular processes with high specificity and sensitivity.
  • Environmental Chemistry: The compound can be applied in environmental monitoring, aiding in the detection of pollutants and contributing to sustainability efforts through its role in developing green chemistry practices.

Citations