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Catalog Number:
40100
CAS Number:
850568-54-6
4-(tert-Butoxycarbonyl)phenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
4-(tert-Butoxycarbonyl)benzeneboronic acid
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$33.75 /200MG
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Product Information

4-(tert-Butoxycarbonyl)phenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals leverage its unique properties to synthesize complex organic molecules, including pharmaceuticals and agrochemicals. Its stability and reactivity under mild conditions allow for efficient coupling reactions, facilitating the development of new compounds with desirable biological activities.

In addition to its synthetic applications, 4-(tert-Butoxycarbonyl)phenylboronic acid serves as a valuable building block in the preparation of various functionalized materials. Its ability to participate in diverse chemical transformations enhances its utility in the development of innovative materials for electronics and catalysis. With its favorable characteristics, this compound stands out as a preferred choice for researchers aiming to streamline their synthetic processes while achieving high yields and purity in their final products.

Synonyms
4-(tert-Butoxycarbonyl)benzeneboronic acid
CAS Number
850568-54-6
Purity
95 - 105% (Assay by titration)
Molecular Formula
C11H15BO4
Molecular Weight
222.05
MDL Number
MFCD03411946
PubChem ID
2773301
Melting Point
106 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-(tert-Butoxycarbonyl)benzeneboronic acid
CAS Number
850568-54-6
Purity
95 - 105% (Assay by titration)
Molecular Formula
C11H15BO4
Molecular Weight
222.05
MDL Number
MFCD03411946
PubChem ID
2773301
Melting Point
106 °C (Lit.)
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

4-(tert-Butoxycarbonyl)phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals, allowing for the creation of complex structures with high efficiency.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds. This application is crucial in the production of fine chemicals and advanced materials.
  • Drug Development: The compound plays a significant role in medicinal chemistry, aiding researchers in the design and synthesis of new drug candidates, particularly those targeting specific biological pathways.
  • Bioconjugation: It is utilized in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules, enhancing the development of targeted therapies and diagnostic tools.
  • Material Science: The compound is also applied in the creation of functional materials, such as sensors and catalysts, benefiting industries focused on innovation in nanotechnology and materials engineering.

Citations