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Catalog Number:
39951
CAS Number:
428820-95-5
2-(3,5-Dinitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
Purity:
≥ 98% (GC)
Synonym(s):
1,3-Dinitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 3,5-Dinitrophenylboronic acid pinacol ester
Documents
$129.19 /200MG
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Product Information

2-(3,5-Dinitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a specialized boron compound that serves as a versatile reagent in organic synthesis and analytical chemistry. This compound is particularly valuable for researchers focusing on the development of new materials and pharmaceuticals due to its unique reactivity and ability to form stable complexes. Its dinitrophenyl group enhances its utility in various applications, including the synthesis of biologically active molecules and the development of fluorescent probes for biological imaging.

The compound's distinctive structure allows it to participate in cross-coupling reactions, making it an essential tool in the synthesis of complex organic compounds. Additionally, its stability and ease of handling make it suitable for both laboratory and industrial applications. Researchers can leverage this compound for its potential in drug discovery and development, as well as in the creation of advanced materials with tailored properties. With its broad range of applications, 2-(3,5-Dinitrophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane stands out as a valuable asset in the toolkit of chemists and material scientists alike.

Synonyms
1,3-Dinitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 3,5-Dinitrophenylboronic acid pinacol ester
CAS Number
428820-95-5
Purity
≥ 98% (GC)
Molecular Formula
C12H15BN2O6
Molecular Weight
294.07
MDL Number
MFCD11504965
PubChem ID
46739239
Melting Point
147 - 151 ?C
Appearance
Light orange to yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
1,3-Dinitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, 3,5-Dinitrophenylboronic acid pinacol ester
CAS Number
428820-95-5
Purity
≥ 98% (GC)
Molecular Formula
C12H15BN2O6
Molecular Weight
294.07
MDL Number
MFCD11504965
PubChem ID
46739239
Melting Point
147 - 151 ?C
Appearance
Light orange to yellow 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

2-(3,5-Dinitrophenyl)-4,4,5,5-tetramethyl-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 various coupling reactions. Its unique structure allows for selective reactivity, making it a valuable tool for chemists.
  • Analytical Chemistry: It is employed in the development of analytical methods for detecting and quantifying phenolic compounds. The dinitrophenyl group enhances the sensitivity and specificity of these methods, which is crucial in environmental monitoring.
  • Pharmaceutical Development: The compound plays a role in drug discovery, particularly in the synthesis of boron-containing pharmaceuticals. Its boron moiety can improve the bioavailability and efficacy of therapeutic agents.
  • Material Science: It is used in the formulation of advanced materials, including polymers and coatings. The incorporation of this compound can enhance the thermal and mechanical properties of materials, making them suitable for high-performance applications.
  • Bioconjugation: This chemical is utilized in bioconjugation techniques, where it helps in attaching biomolecules to surfaces or other molecules. This application is significant in the development of biosensors and targeted drug delivery systems.

Citations