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Catalog Number:
39894
CAS Number:
594823-67-3
2-(3-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
1-Bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 3-Bromophenylboronic acid pinacol ester
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$58.39 /1G
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Product Information

2-(3-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile organoboron compound that has garnered attention in various fields, particularly in organic synthesis and medicinal chemistry. This compound is recognized for its unique ability to facilitate the formation of carbon-carbon bonds, making it an essential reagent in cross-coupling reactions such as Suzuki-Miyaura coupling. Its bromophenyl group enhances its reactivity and selectivity, allowing for the efficient synthesis of complex organic molecules, which is invaluable in drug discovery and development.

Researchers and industry professionals can leverage this compound's properties to streamline synthetic pathways, reduce reaction times, and improve yields in the production of pharmaceuticals and agrochemicals. Additionally, its stability and ease of handling make it an attractive option for both laboratory and industrial applications. The incorporation of this compound into synthetic methodologies not only enhances efficiency but also opens avenues for the development of novel compounds with potential therapeutic applications.

Synonyms
1-Bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 3-Bromophenylboronic acid pinacol ester
CAS Number
594823-67-3
Purity
≥ 98% (GC)
Molecular Formula
C12H16BBrO2
Molecular Weight
282.97
MDL Number
MFCD12545926
PubChem ID
9993953
Melting Point
46 - 50 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
1-Bromo-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 3-Bromophenylboronic acid pinacol ester
CAS Number
594823-67-3
Purity
≥ 98% (GC)
Molecular Formula
C12H16BBrO2
Molecular Weight
282.97
MDL Number
MFCD12545926
PubChem ID
9993953
Melting Point
46 - 50 ?C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-(3-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 organic chemistry, particularly in the synthesis of complex molecules, enabling chemists to create new compounds efficiently.
  • Pharmaceutical Development: It plays a crucial role in drug discovery, acting as an intermediate in the synthesis of pharmaceutical agents, which can lead to the development of new medications.
  • Material Science: The compound is used in the formulation of advanced materials, such as polymers and coatings, enhancing their properties like durability and resistance to environmental factors.
  • Analytical Chemistry: It is utilized in analytical applications, including chromatography and mass spectrometry, helping researchers identify and quantify various substances in complex mixtures.
  • Environmental Monitoring: This chemical can be employed in the detection and analysis of pollutants, aiding in environmental assessments and ensuring compliance with safety regulations.

Citations