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331273-58-6

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

Catalog#: AR01DL81  |   CAS#: 331273-58-6  |   MDL#: MFCD16994282  |   MF: C13H19BO3  |   MW: 234.0992

Packsize Purity Price Availability Quantity
50mg 95% $303.00 2-3 weeks Buy Now Add To Cart
100mg 95% $439.00 2-3 weeks Buy Now Add To Cart
250mg 95% $618.00 2-3 weeks Buy Now Add To Cart
500mg 95% $959.00 2-3 weeks Buy Now Add To Cart
1g 95% $1,223.00 2-3 weeks Buy Now Add To Cart
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Catalog Number AR01DL81
Chemical Name 2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
CAS Number 331273-58-6
Molecular Formula C13H19BO3
Molecular Weight 234.0992
MDL Number MFCD16994282
SMILES Cc1ccc(cc1O)B1OC(C(O1)(C)C)(C)C

2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol, often referred to as $name$, serves as a crucial component in chemical synthesis processes. This compound plays a vital role as a versatile building block with remarkable reactivity and selectivity characteristics. In the realm of chemical synthesis, $name$ is commonly employed as a key reagent in Suzuki-Miyaura cross-coupling reactions.This specific application leads to the formation of complex organic molecules by facilitating the coupling of aryl halides or pseudohalides with various boronic acid derivatives. Through this process, $name$ enables the construction of C-C bonds, a fundamental step in the creation of pharmaceuticals, agrochemicals, and materials of interest in academic and industrial research settings.In addition to its utility in Suzuki-Miyaura coupling, 2-Methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenol also exhibits compatibility with a range of functional groups, enhancing its applicability in diverse synthetic strategies. By leveraging the unique properties of $name$, chemists can efficiently access novel molecular structures and advance the frontier of organic synthesis.
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GHS Pictogram N/A
UN# -
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