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Catalog Number:
40055
CAS Number:
195062-61-4
2-(4-clorofenil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano
Purity:
≥ 98% (GC)
Synonym(s):
1-Cloro-4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)benceno, Éster de pinacol del ácido 4-clorofenilborónico
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Product Information

2-(4-Chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile chemical 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 an effective reagent in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for the formation of carbon-carbon bonds. Its ability to facilitate the synthesis of complex organic molecules makes it a crucial tool for researchers in pharmaceuticals and materials science.

Additionally, the presence of the chlorophenyl group contributes to its utility in the development of agrochemicals and fine chemicals, where it can be employed to create novel compounds with specific biological activities. The compound's high stability and ease of handling further enhance its appeal, making it an excellent choice for both laboratory and industrial applications. With its broad range of uses, 2-(4-Chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane stands out as a key ingredient for innovative chemical processes.

Synonyms
1-Cloro-4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)benceno, Éster de pinacol del ácido 4-clorofenilborónico
CAS Number
195062-61-4
Purity
≥ 98% (GC)
Molecular Formula
C12H16BClO2
Molecular Weight
238.52
MDL Number
MFCD05663875
PubChem ID
10633712
Melting Point
53 - 57 °C
Density
1,10 g/ml
Appearance
Polvo cristalino de color blanco a blanquecino.
Boiling Point
317,89 °C (Literatura)
Refractive Index
n20D 1,50
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
1-Cloro-4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)benceno, Éster de pinacol del ácido 4-clorofenilborónico
CAS Number
195062-61-4
Purity
≥ 98% (GC)
Molecular Formula
C12H16BClO2
Molecular Weight
238.52
MDL Number
MFCD05663875
PubChem ID
10633712
Melting Point
53 - 57 °C
Density
1,10 g/ml
Appearance
Polvo cristalino de color blanco a blanquecino.
Boiling Point
317,89 °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

2-(4-Chlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic synthesis, particularly in the formation of carbon-carbon bonds, making it invaluable for chemists developing new pharmaceuticals and agrochemicals.
  • Drug Development: Its unique structure allows for the modification of drug candidates, enhancing their efficacy and selectivity. Researchers in the pharmaceutical industry leverage this to create more effective treatments.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and coatings, where its properties can improve durability and performance in various applications.
  • Analytical Chemistry: It acts as a reagent in analytical methods, aiding in the detection and quantification of specific compounds, which is crucial for quality control in manufacturing processes.
  • Environmental Applications: The compound can be utilized in the synthesis of environmentally friendly chemicals, contributing to sustainable practices in industries like agriculture and waste management.

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