Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
40003
CAS Number:
68716-49-4
2-(4-bromofenil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano
Purity:
≥ 98% (GC)
Synonym(s):
1-Bromo-4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)benceno, Éster de pinacol del ácido 4-bromofenilborónico
Documents
$73.71 /1G
Tamaño
Request Bulk Quote
Product Information

2-(4-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile boron-containing compound known for its unique properties and applications in organic synthesis and materials science. This compound serves as an effective reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which is crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Its high stability and selectivity make it an ideal choice for researchers looking to synthesize complex organic molecules with precision.

Additionally, the presence of the bromophenyl group enhances its reactivity, allowing for a wide range of functionalization possibilities. This compound is particularly valuable in the synthesis of biologically active compounds and can be utilized in the production of OLED materials due to its favorable electronic properties. Researchers and industry professionals will appreciate its efficiency and reliability in various applications, making it a preferred choice for innovative chemical synthesis.

Synonyms
1-Bromo-4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)benceno, Éster de pinacol del ácido 4-bromofenilborónico
CAS Number
68716-49-4
Purity
≥ 98% (GC)
Molecular Formula
C12H16BBrO2
Molecular Weight
282.97
MDL Number
MFCD11110553
PubChem ID
10755376
Melting Point
69 - 73 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
1-Bromo-4-(4,4,5,5-tetrametil-1,3,2-dioxaborolan-2-il)benceno, Éster de pinacol del ácido 4-bromofenilborónico
CAS Number
68716-49-4
Purity
≥ 98% (GC)
Molecular Formula
C12H16BBrO2
Molecular Weight
282.97
MDL Number
MFCD11110553
PubChem ID
10755376
Melting Point
69 - 73 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-(4-Bromophenyl)-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 the synthesis of various organic molecules, particularly in the formation of carbon-carbon bonds, making it invaluable for chemists in developing new pharmaceuticals and agrochemicals.
  • Drug Development: Its unique properties allow for the modification of drug candidates, enhancing their efficacy and selectivity. Researchers in medicinal chemistry often use it to create more effective therapeutic agents.
  • Material Science: It is employed in the production of advanced materials, such as polymers and nanomaterials, where its boron content contributes to improved mechanical and thermal properties.
  • Fluorescent Probes: The compound can be utilized in the design of fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes with high specificity and sensitivity.
  • Catalysis: It acts as a catalyst in various chemical reactions, offering advantages like increased reaction rates and selectivity, which are crucial for industrial applications in chemical manufacturing.

Citas