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Home  > 4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

AA32797

1196985-65-5 | 4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol

Packsize Purity Availability Price Discounted Price    Quantity
250mg 95% in stock $114.00 $80.00 -   +
1g 95% in stock $235.00 $165.00 -   +
5g 95% in stock $775.00 $543.00 -   +
10g 95% in stock $1,319.00 $923.00 -   +
25g 95% in stock $2,625.00 $1,837.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AA32797
Chemical Name: 4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
CAS Number: 1196985-65-5
Molecular Formula: C13H19BO3
Molecular Weight: 234.09915999999996
MDL Number: MFCD16994425
SMILES: CC1(C)OB(OC1(C)C)c1cc(O)ccc1C

 

Upstream Synthesis Route
  • 4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol, commonly known as $name$, is a valuable chemical compound widely utilized in the field of chemical synthesis. Due to its unique structural features, this compound is highly sought after for its versatile applications in organic chemistry.One crucial role of 4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol is its function as a key building block in the synthesis of various pharmaceuticals, agrochemicals, and organic materials. Its incorporation into synthetic pathways enables the selective introduction of the phenolic moiety in target molecules with high efficiency and precision.Furthermore, 4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol serves as a valuable reagent in C–C bond formation reactions, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. This compound's boron-containing group plays a pivotal role in facilitating C–C bond formation, making it an indispensable tool for the construction of complex organic frameworks.In addition to its synthetic utility, 4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol also finds application in material science, where its incorporation into polymer structures imparts desirable properties such as improved thermal stability and functionality. Its versatility and compatibility with various synthetic methodologies make it a valuable asset in the arsenal of chemists and researchers working in the field of chemical synthesis.
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