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Catalog Number:
39991
CAS Number:
190788-59-1
4,4,5,5-tétraméthyl-2-(2-nitrophényl)-1,3,2-dioxaborolane
Purity:
≥ 98% (CG)
Synonym(s):
1-Nitro-2-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzène, Ester pinacolique de l'acide 2-nitrophénylboronique
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Product Information

4,4,5,5-Tetramethyl-2-(2-nitrophenyl)-1,3,2-dioxaborolane is a specialized boron-containing compound recognized for its unique properties and versatility in various applications. This compound features a dioxaborolane structure, which enhances its stability and reactivity, making it an excellent candidate for use in organic synthesis and materials science. Its nitrophenyl group contributes to its potential as a building block in the development of advanced materials, pharmaceuticals, and agrochemicals.

Researchers and industry professionals can leverage 4,4,5,5-Tetramethyl-2-(2-nitrophenyl)-1,3,2-dioxaborolane for its role in cross-coupling reactions, particularly in the formation of carbon-carbon bonds, which is essential in the synthesis of complex organic molecules. Additionally, its application in the development of sensors and electronic materials showcases its relevance in cutting-edge research. The compound's unique structure not only enhances its reactivity but also provides a pathway for the creation of innovative products in various fields, including medicinal chemistry and polymer science.

Synonyms
1-Nitro-2-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzène, Ester pinacolique de l'acide 2-nitrophénylboronique
CAS Number
190788-59-1
Purity
≥ 98% (CG)
Molecular Formula
C 12 H 16 BNO 4
Molecular Weight
249.07
MDL Number
MFCD02179447
PubChem ID
3699568
Melting Point
45 - 49 ?C
Appearance
Poudre cristalline blanche à orange
Conditions
Magasin chez RT
General Information
Synonyms
1-Nitro-2-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)benzène, Ester pinacolique de l'acide 2-nitrophénylboronique
CAS Number
190788-59-1
Purity
≥ 98% (CG)
Molecular Formula
C 12 H 16 BNO 4
Molecular Weight
249.07
MDL Number
MFCD02179447
PubChem ID
3699568
Melting Point
45 - 49 ?C
Appearance
Poudre cristalline blanche à orange
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

4,4,5,5-Tetramethyl-2-(2-nitrophenyl)-1,3,2-dioxaborolane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, facilitating the formation of complex molecules through its unique reactivity, especially in cross-coupling reactions.
  • Fluorescent Probes: It is employed in the development of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high specificity and sensitivity.
  • Drug Development: The compound plays a role in medicinal chemistry, where it is used to modify drug candidates, enhancing their efficacy and selectivity in targeting specific biological pathways.
  • Environmental Monitoring: It can be utilized in the detection of pollutants, providing a method for monitoring environmental health and safety through its chemical properties.
  • Material Science: This chemical is applied in the synthesis of advanced materials, such as polymers and nanomaterials, which have applications in electronics and renewable energy technologies.

Citations