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Catalog Number:
40046
CAS Number:
480424-70-2
Acetato de 4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)fenilo
Purity:
≥ 96% (GC)
Synonym(s):
Éster de pinacol del ácido 4-acetoxifenilborónico, 2-(4-Acetoxifenil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano
Documents
$79.22 /1G
Tamaño
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Product Information

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl acetate is a versatile compound that serves as a valuable building block in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its unique dioxaborolane structure enhances its reactivity, making it an excellent candidate for cross-coupling reactions, which are essential in the formation of carbon-carbon bonds. This compound is particularly useful in the synthesis of complex organic molecules, allowing researchers to create novel compounds with tailored properties for specific applications.

In addition to its synthetic utility, 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl acetate is recognized for its stability and ease of handling, which are crucial for laboratory environments. Its application in medicinal chemistry has shown promise in the development of new therapeutic agents, while its role in material science is being explored for creating advanced materials with unique functionalities. This compound stands out for its ability to facilitate efficient and selective reactions, making it a preferred choice for researchers aiming to optimize their synthetic pathways.

Synonyms
Éster de pinacol del ácido 4-acetoxifenilborónico, 2-(4-Acetoxifenil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano
CAS Number
480424-70-2
Purity
≥ 96% (GC)
Molecular Formula
C 14 H 19 BO 4
Molecular Weight
262.11
MDL Number
MFCD03453060
PubChem ID
2774004
Melting Point
66 - 72 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
Éster de pinacol del ácido 4-acetoxifenilborónico, 2-(4-Acetoxifenil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano
CAS Number
480424-70-2
Purity
≥ 96% (GC)
Molecular Formula
C 14 H 19 BO 4
Molecular Weight
262.11
MDL Number
MFCD03453060
PubChem ID
2774004
Melting Point
66 - 72 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en 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)phenyl acetate is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, facilitating the synthesis of various complex molecules, which is crucial for pharmaceutical development.
  • Medicinal Chemistry: Its unique structure allows for the modification of drug candidates, enhancing their efficacy and bioavailability, making it valuable in the design of new therapeutic agents.
  • Material Science: Used in the development of advanced materials, this compound contributes to the creation of polymers and coatings with improved properties, such as durability and resistance to environmental factors.
  • Bioconjugation: The compound's functional groups enable it to be used in bioconjugation processes, aiding in the development of targeted drug delivery systems and diagnostic tools in biotechnology.
  • Fluorescent Probes: It is employed in the creation of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes in real-time, which is essential for understanding disease mechanisms.

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