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Catalog Number:
39878
CAS Number:
889865-38-7
4,4,5,5-Tetramethyl-2-[4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]-1,3,2-dioxaborolane
Purity:
≥ 96% (GC)
Synonym(s):
2-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolane-2-yl)phenoxy]tetrahydro-2H-pyran, 4-[(Tetrahydro-2H-pyran-2-yl)oxy]phenylboronic acid pinacol ester
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Product Information

4,4,5,5-Tetramethyl-2-[4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]-1,3,2-dioxaborolane is a versatile boron-containing compound that has garnered attention in various fields, particularly in organic synthesis and materials science. This compound is recognized for its unique structural features, including a dioxaborolane ring, which enhances its reactivity and stability. Its ability to act as a boron source makes it invaluable in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds essential for creating complex organic molecules.

Moreover, its application extends to the development of advanced materials, such as polymers and coatings, where it can improve mechanical properties and thermal stability. Researchers are increasingly exploring its potential in drug delivery systems and as a building block in the synthesis of pharmaceuticals, owing to its favorable solubility and functionalization capabilities. With its multifunctional properties, 4,4,5,5-Tetramethyl-2-[4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]-1,3,2-dioxaborolane stands out as a promising compound for innovative applications in both academic and industrial settings.

Synonyms
2-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolane-2-yl)phenoxy]tetrahydro-2H-pyran, 4-[(Tetrahydro-2H-pyran-2-yl)oxy]phenylboronic acid pinacol ester
CAS Number
889865-38-7
Purity
≥ 96% (GC)
Molecular Formula
C17H25BO4
Molecular Weight
304.19
MDL Number
MFCD06659834
PubChem ID
58005653
Melting Point
57 - 61 ?C
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolane-2-yl)phenoxy]tetrahydro-2H-pyran, 4-[(Tetrahydro-2H-pyran-2-yl)oxy]phenylboronic acid pinacol ester
CAS Number
889865-38-7
Purity
≥ 96% (GC)
Molecular Formula
C17H25BO4
Molecular Weight
304.19
MDL Number
MFCD06659834
PubChem ID
58005653
Melting Point
57 - 61 ?C
Appearance
White to light 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

4,4,5,5-Tetramethyl-2-[4-[(tetrahydro-2H-pyran-2-yl)oxy]phenyl]-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.
  • Pharmaceutical Development: It plays a crucial role in the synthesis of pharmaceutical intermediates, aiding in the development of new drugs with enhanced efficacy and reduced side effects.
  • Material Science: The compound is used in the creation of advanced materials, such as polymers and coatings, that exhibit improved durability and chemical resistance.
  • Bioconjugation: Its unique structure allows for effective bioconjugation processes, making it valuable in the development of targeted drug delivery systems and diagnostic tools.
  • Environmental Applications: The compound can be utilized in the synthesis of environmentally friendly chemicals, contributing to sustainable practices in various industries.

Citations