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Catalog Number:
39898
CAS Number:
269410-06-2
2-(2-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 97% (Assay by titration)
Synonym(s):
1-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 2-Bromophenylboronic acid pinacol ester
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Product Information

2-(2-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 participate in cross-coupling reactions, making it an invaluable tool for researchers aiming to create complex organic molecules. Its structure, featuring a bromophenyl group, enhances its reactivity, allowing for efficient transformations in the development of pharmaceuticals and agrochemicals.

In addition to its synthetic applications, this compound serves as a key intermediate in the preparation of biologically active compounds, including potential drug candidates. Its stability and ease of handling make it suitable for both laboratory and industrial settings. Researchers can leverage its properties to streamline their synthesis processes, ultimately leading to more efficient production of target molecules. With its growing relevance in the field of materials science and nanotechnology, 2-(2-Bromophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane stands out as a compound with significant potential for innovation and discovery.

Synonyms
1-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 2-Bromophenylboronic acid pinacol ester
CAS Number
269410-06-2
Purity
≥ 97% (Assay by titration)
Molecular Formula
C12H16BBrO2
Molecular Weight
282.97
MDL Number
MFCD08276318
PubChem ID
21923944
Appearance
Slightly yellow to orange clear liquid
Conditions
Store at RT
General Information
Synonyms
1-Bromo-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 2-Bromophenylboronic acid pinacol ester
CAS Number
269410-06-2
Purity
≥ 97% (Assay by titration)
Molecular Formula
C12H16BBrO2
Molecular Weight
282.97
MDL Number
MFCD08276318
PubChem ID
21923944
Appearance
Slightly yellow to orange clear liquid
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-(2-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 building block in organic chemistry, particularly in the synthesis of complex molecules, making it invaluable for researchers in pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is often employed in Suzuki-Miyaura coupling reactions, facilitating the formation of carbon-carbon bonds, which is crucial for developing new materials and drugs.
  • Fluorescent Probes: The compound can be used to create fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes and structures in real-time.
  • Material Science: Its unique properties allow for applications in the development of advanced materials, such as polymers and nanomaterials, which are essential in electronics and renewable energy technologies.
  • Environmental Chemistry: This chemical can be utilized in the detection and removal of pollutants, contributing to environmental monitoring and remediation efforts.

Citations