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Catalog Number:
40167
CAS Number:
195062-62-5
4-(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)benzoato de etilo
Purity:
≥ 96% (GC)
Synonym(s):
Éster etílico del ácido 4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)benzoico, Éster de pinacol del ácido 4-etoxicarbonilfenilborónico
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$88.93 /1G
Tamaño
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Product Information

Ethyl 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This compound features a unique dioxaborolane moiety, which enhances its reactivity and selectivity in various chemical reactions, making it an invaluable tool for researchers and industry professionals. Its structure allows for efficient coupling reactions, particularly in the development of complex organic molecules, including pharmaceuticals and agrochemicals.

The compound's stability and functionalization potential make it ideal for applications in the synthesis of biologically active compounds, where precision and efficiency are paramount. Additionally, its use in cross-coupling reactions can lead to the creation of novel materials with tailored properties, appealing to those in materials science and polymer chemistry. Ethyl 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate stands out for its ability to facilitate reactions that are often challenging with traditional reagents, thus streamlining workflows and enhancing productivity in research and industrial settings.

Synonyms
Éster etílico del ácido 4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)benzoico, Éster de pinacol del ácido 4-etoxicarbonilfenilborónico
CAS Number
195062-62-5
Purity
≥ 96% (GC)
Molecular Formula
C 15 H 21 BO 4
Molecular Weight
276.14
MDL Number
MFCD03453659
PubChem ID
2734618
Density
1,05 g/mL a 25 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Boiling Point
330 °C (Literatura)
Refractive Index
n20D 1,50
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Éster etílico del ácido 4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)benzoico, Éster de pinacol del ácido 4-etoxicarbonilfenilborónico
CAS Number
195062-62-5
Purity
≥ 96% (GC)
Molecular Formula
C 15 H 21 BO 4
Molecular Weight
276.14
MDL Number
MFCD03453659
PubChem ID
2734618
Density
1,05 g/mL a 25 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Boiling Point
330 °C (Literatura)
Refractive Index
n20D 1,50
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethyl 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: It is employed in the design and optimization of drug candidates, where its unique boron-containing structure can enhance biological activity and selectivity.
  • Material Science: The compound is used in the formulation of advanced materials, such as polymers and coatings, which benefit from its chemical stability and reactivity.
  • Fluorescent Probes: It can be utilized in creating fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high specificity.
  • Cross-Coupling Reactions: This chemical plays a crucial role in cross-coupling reactions, which are essential for forming carbon-carbon bonds in various synthetic pathways, making it a valuable tool for chemists.

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