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Catalog Number:
40004
CAS Number:
166330-03-6
2-(Bromomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (NMR)
Synonym(s):
(Bromomethyl)boronic acid pinacol ester
Documents
$25.04 /1G
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Product Information

2-(Bromomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile chemical compound that plays a significant role in organic synthesis and materials science. This compound is recognized for its unique dioxaborolane structure, which enhances its reactivity and stability, making it an ideal candidate for various applications. It is particularly useful in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals, due to its ability to facilitate carbon-carbon bond formation. Researchers appreciate its utility in cross-coupling reactions, which are essential in the development of new materials and compounds.

In addition to its synthetic applications, 2-(Bromomethyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is also employed in the production of functionalized polymers and advanced materials. Its unique properties allow for the modification of polymer backbones, leading to materials with tailored functionalities. This compound stands out for its ease of handling and compatibility with various reaction conditions, making it a preferred choice for both academic and industrial laboratories. Whether you are developing new pharmaceuticals or innovative materials, this compound offers the reliability and performance needed for successful outcomes.

Synonyms
(Bromomethyl)boronic acid pinacol ester
CAS Number
166330-03-6
Purity
≥ 98% (NMR)
Molecular Formula
C7H14BBrO2
Molecular Weight
220.9
MDL Number
MFCD09271779
PubChem ID
10955110
Density
1.26 g/mL
Appearance
Colorless to light yellow liquid
Conditions
Store at 2 - 8 °C
General Information
Synonyms
(Bromomethyl)boronic acid pinacol ester
CAS Number
166330-03-6
Purity
≥ 98% (NMR)
Molecular Formula
C7H14BBrO2
Molecular Weight
220.9
MDL Number
MFCD09271779
PubChem ID
10955110
Density
1.26 g/mL
Appearance
Colorless to light yellow liquid
Conditions
Store at 2 - 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-(Bromomethyl)-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, enabling the synthesis of various complex molecules, particularly in the pharmaceutical industry.
  • Cross-Coupling Reactions: It is employed in palladium-catalyzed cross-coupling reactions, which are essential for forming carbon-carbon bonds, making it valuable for developing new materials and drugs.
  • Bioconjugation: The unique reactivity of this compound allows for bioconjugation applications, where it can be used to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Polymer Chemistry: It is utilized in the modification of polymers, improving their properties for applications in coatings, adhesives, and other materials, thus enhancing performance and durability.
  • Research in Catalysis: This compound is significant in catalytic research, helping scientists explore new catalytic processes that can lead to more efficient chemical reactions, reducing waste and energy consumption.

Citations