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Catalog Number:
39910
CAS Number:
171364-85-5
3-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)quinoléine
Purity:
≥ 98% (CG)
Synonym(s):
4,4,5,5-tétraméthyl-2-(3-quinolyl)-1,3,2-dioxaborolane, Ester pinacol de l'acide quinoléine-3-boronique
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Product Information

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline is a versatile compound that combines the unique properties of quinoline with the stability and reactivity of a dioxaborolane moiety. This compound is particularly valuable in organic synthesis and medicinal chemistry, where it serves as a key intermediate in the development of various pharmaceuticals and agrochemicals. Its ability to participate in cross-coupling reactions makes it an essential building block for creating complex molecular architectures, which are crucial in drug discovery and development.

Researchers and industry professionals appreciate this compound for its enhanced solubility and stability, which can lead to improved reaction yields and efficiency. Its applications extend to the synthesis of biologically active compounds, where it can facilitate the introduction of boron into organic molecules, thus enabling further functionalization. With its unique structural features, 3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline stands out as a valuable tool in the arsenal of synthetic chemists, offering both practicality and versatility in various chemical applications.

Synonyms
4,4,5,5-tétraméthyl-2-(3-quinolyl)-1,3,2-dioxaborolane, Ester pinacol de l'acide quinoléine-3-boronique
CAS Number
171364-85-5
Purity
≥ 98% (CG)
Molecular Formula
C 15 H 18 BNO 2
Molecular Weight
255.12
MDL Number
MFCD05155218
PubChem ID
10848590
Melting Point
58 - 62 ?C
Appearance
Poudre cristalline blanche à orange
Conditions
Conserver entre 2 et 8 °C
General Information
Synonyms
4,4,5,5-tétraméthyl-2-(3-quinolyl)-1,3,2-dioxaborolane, Ester pinacol de l'acide quinoléine-3-boronique
CAS Number
171364-85-5
Purity
≥ 98% (CG)
Molecular Formula
C 15 H 18 BNO 2
Molecular Weight
255.12
MDL Number
MFCD05155218
PubChem ID
10848590
Melting Point
58 - 62 ?C
Appearance
Poudre cristalline blanche à orange
Conditions
Conserver entre 2 et 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, facilitating the synthesis of complex molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Fluorescent Probes: Its unique structure allows it to be used in the creation of fluorescent probes for biological imaging, enhancing the visualization of cellular processes in research and diagnostics.
  • Drug Development: The compound's properties make it valuable in the design of new drug candidates, especially in targeting specific biological pathways, which can lead to more effective treatments.
  • Materials Science: It is applied in the development of advanced materials, including polymers and nanomaterials, which can be used in electronics and coatings, offering improved performance and durability.
  • Environmental Applications: This chemical can be utilized in the development of sensors for detecting environmental pollutants, aiding in monitoring and protecting ecosystems.

Citations