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Catalog Number:
39881
CAS Number:
302348-51-2
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl alcohol
Purity:
≥ 98% (GC)
Synonym(s):
2-[4-(Hydroxymethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 4-(Hydroxymethyl)phenylboronic acid pinacol ester
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Product Information

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl alcohol is a versatile compound known for its unique boron-containing structure, which enhances its reactivity and utility in various applications. This compound is particularly valuable in organic synthesis, where it serves as a key intermediate in the development of pharmaceuticals and agrochemicals. Its ability to participate in cross-coupling reactions makes it an essential building block for creating complex molecular architectures. Researchers appreciate its stability and ease of handling, which facilitate its use in laboratory settings.

In addition to its synthetic applications, this compound has shown promise in materials science, particularly in the development of boron-doped polymers and advanced materials. Its unique properties allow for enhanced performance in electronic applications, such as organic light-emitting diodes (OLEDs) and sensors. By incorporating 4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl alcohol into their formulations, professionals can achieve improved efficiency and functionality in their products, making it a valuable addition to any research or industrial portfolio.

Synonyms
2-[4-(Hydroxymethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 4-(Hydroxymethyl)phenylboronic acid pinacol ester
CAS Number
302348-51-2
Purity
≥ 98% (GC)
Molecular Formula
C13H19BO3
Molecular Weight
234.1
MDL Number
MFCD09837617
PubChem ID
11402050
Melting Point
74 - 78 ?C
Appearance
White to light yellow crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
2-[4-(Hydroxymethyl)phenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 4-(Hydroxymethyl)phenylboronic acid pinacol ester
CAS Number
302348-51-2
Purity
≥ 98% (GC)
Molecular Formula
C13H19BO3
Molecular Weight
234.1
MDL Number
MFCD09837617
PubChem ID
11402050
Melting Point
74 - 78 ?C
Appearance
White to light yellow crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the production of pharmaceuticals and agrochemicals.
  • Drug Development: It plays a crucial role in medicinal chemistry, where it can be used to modify drug candidates, enhancing their efficacy and selectivity in targeting specific biological pathways.
  • Material Science: The compound is valuable in the development of advanced materials, including polymers and coatings, due to its unique chemical properties that improve material performance.
  • Fluorescent Probes: It can be employed in the creation of fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high specificity.
  • Catalysis: This chemical is also used in catalytic processes, facilitating various chemical reactions with improved efficiency compared to traditional catalysts.

Citations