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Catalog Number:
23333
CAS Number:
1315476-05-1
Ácido 5-cloro-2-[(2,2-dimetilpropoxi)carbonil]fenil)borónico
Synonym(s):
Ácido 2,2-dimetilpropil-4'-clorobenzoato-2'-borónico
Documents
$146.92 /100 mg
Tamaño
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Product Information

(5-Chloro-2-[(2,2-dimethylpropoxy)carbonyl]phenyl)boronic acid is a versatile boronic acid derivative that plays a significant 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 synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure, featuring a chloro group and a dimethylpropoxycarbonyl moiety, enhances its reactivity and selectivity, allowing for the efficient formation of carbon-carbon bonds. Researchers and industry professionals can leverage this compound in the development of targeted therapies and innovative materials, showcasing its potential in drug discovery and material science.

The practical applications of (5-Chloro-2-[(2,2-dimethylpropoxy)carbonyl]phenyl)boronic acid extend to the synthesis of biologically active compounds, where it serves as a crucial intermediate. Its compatibility with various reaction conditions and substrates makes it a preferred choice for chemists looking to streamline their synthetic pathways. By integrating this compound into their workflows, professionals can achieve higher yields and improved purity in their final products, ultimately enhancing the efficiency of their research and development processes.

Synonyms
Ácido 2,2-dimetilpropil-4'-clorobenzoato-2'-borónico
CAS Number
1315476-05-1
Molecular Formula
C12H16BClO4
Molecular Weight
270.52
MDL Number
MFCD01631848
PubChem ID
44784947
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido 2,2-dimetilpropil-4'-clorobenzoato-2'-borónico
CAS Number
1315476-05-1
Molecular Formula
C12H16BClO4
Molecular Weight
270.52
MDL Number
MFCD01631848
PubChem ID
44784947
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-Chloro-2-[(2,2-dimethylpropoxy)carbonyl]phenyl)boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting specific diseases, enhancing their efficacy and selectivity.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki reactions, which are essential for creating complex organic molecules, making it invaluable in the field of organic chemistry.
  • Material Science: The compound is used in the fabrication of advanced materials, including polymers and nanomaterials, which have applications in electronics and coatings, providing improved performance and durability.
  • Bioconjugation: It plays a role in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial in the development of biosensors and targeted drug delivery systems.
  • Environmental Chemistry: This chemical is also investigated for its potential in environmental applications, such as the removal of pollutants, due to its reactivity and ability to form stable complexes with various contaminants.

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