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Catalog Number:
39970
CAS Number:
269410-25-5
2,6-Diméthyl-4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)phénol
Purity:
≥ 98% (CG)
Synonym(s):
2-(4-hydroxy-3,5-diméthylphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, 4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)-2,6-xylénol, Ester pinacol de l'acide 4-hydroxy-3,5-diméthylphénylboronique
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Product Information

2,6-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol is a versatile compound known for its unique boron-containing structure, which enhances its utility in various chemical applications. This compound serves as an important intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its ability to participate in cross-coupling reactions makes it invaluable for researchers looking to create complex molecular architectures. Additionally, the presence of the dioxaborolane moiety allows for improved stability and selectivity in reactions, making it a preferred choice for chemists aiming for high yields and efficiency.

In the field of materials science, this compound can be utilized in the formulation of advanced materials, including polymers and coatings, due to its favorable chemical properties. Its unique structure not only contributes to enhanced performance but also opens avenues for innovation in product development. Researchers and industry professionals can leverage the advantages of 2,6-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol to drive their projects forward, ensuring they remain at the forefront of their respective fields.

Synonyms
2-(4-hydroxy-3,5-diméthylphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, 4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)-2,6-xylénol, Ester pinacol de l'acide 4-hydroxy-3,5-diméthylphénylboronique
CAS Number
269410-25-5
Purity
≥ 98% (CG)
Molecular Formula
C 14 H 21 BO 3
Molecular Weight
248.13
MDL Number
MFCD02093724
PubChem ID
2734649
Melting Point
106 - 110 ?C
Conditions
Magasin chez RT
General Information
Synonyms
2-(4-hydroxy-3,5-diméthylphényl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane, 4-(4,4,5,5-tétraméthyl-1,3,2-dioxaborolan-2-yl)-2,6-xylénol, Ester pinacol de l'acide 4-hydroxy-3,5-diméthylphénylboronique
CAS Number
269410-25-5
Purity
≥ 98% (CG)
Molecular Formula
C 14 H 21 BO 3
Molecular Weight
248.13
MDL Number
MFCD02093724
PubChem ID
2734649
Melting Point
106 - 110 ?C
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

2,6-Dimethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol 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 through various coupling reactions.
  • Medicinal Chemistry: It plays a crucial role in the development of pharmaceuticals, particularly in the design of compounds with enhanced biological activity and specificity.
  • Material Science: The chemical is used in the formulation of advanced materials, including polymers and coatings, that require specific thermal and mechanical properties.
  • Catalysis: It acts as a ligand in catalytic processes, improving reaction efficiencies and selectivities in various chemical transformations.
  • Analytical Chemistry: This compound is employed in the development of sensors and probes for detecting specific analytes, enhancing the sensitivity and accuracy of measurements.

Citations