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Catalog Number:
23331
CAS Number:
1309980-79-7
Ácido 5-bromo-2-[(2,2-dimetilpropoxi)carbonil]fenil)borónico
Synonym(s):
Ácido 2,2-dimetilpropil-4'-bromobenzoato-2'-borónico
Documents
$146.92 /100 mg
Tamaño
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Product Information

(5-Bromo-2-[(2,2-dimethylpropoxy)carbonyl]phenyl)boronic acid is a versatile boronic acid derivative that plays a crucial role in organic synthesis and medicinal chemistry. This compound is particularly valued for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of biaryl compounds. Its unique structure, featuring a bromine atom and a bulky 2,2-dimethylpropoxycarbonyl group, enhances its reactivity and selectivity in various coupling reactions, which are pivotal in the development of pharmaceuticals and agrochemicals.

Researchers and industry professionals can leverage this compound for the synthesis of complex organic molecules, including potential drug candidates and advanced materials. Its stability and compatibility with a range of reaction conditions make it an attractive choice for both laboratory and industrial applications. Additionally, the compound's ability to facilitate the formation of carbon-carbon bonds opens up new avenues for innovation in chemical synthesis, providing significant advantages over traditional methods.

Synonyms
Ácido 2,2-dimetilpropil-4'-bromobenzoato-2'-borónico
CAS Number
1309980-79-7
Molecular Formula
C12H16BBrO4
Molecular Weight
314.97
MDL Number
MFCD01631844
PubChem ID
44784945
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido 2,2-dimetilpropil-4'-bromobenzoato-2'-borónico
CAS Number
1309980-79-7
Molecular Formula
C12H16BBrO4
Molecular Weight
314.97
MDL Number
MFCD01631844
PubChem ID
44784945
Conditions
Conservar entre 0 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

(5-Bromo-2-[(2,2-dimethylpropoxy)carbonyl]phenyl)boronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the pharmaceutical industry where it aids in developing new drugs.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in organic compounds, making it invaluable for chemists working on material science and drug discovery.
  • Bioconjugation: The boronic acid functional group allows for selective binding to diols, making it useful in bioconjugation processes, such as attaching drugs to antibodies for targeted therapy in cancer treatment.
  • Sensor Development: This compound can be employed in the development of chemical sensors for detecting glucose and other biomolecules, benefiting the medical and health monitoring industries.
  • Polymer Chemistry: It is also used in the modification of polymers, enhancing their properties for applications in coatings, adhesives, and other materials, thus improving performance and durability.

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