Catalog Number | ACM159191567 |
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CAS Number | 159191-56-7 |
Structure | |
Synonyms | 4-(T-BUTYL DIMETHYLSILOXY) PHENYL BORONIC ACID;4-(TERT-BUTYL DIMETHYLSILOXY)PHENYL BORONIC ACID;4-(TERT-BUTYLDIMETHYLSILYLOXY)PHENYLBORONIC ACID;4-(TERT-BUTYLDIMETHYLSILYOXY)PHENYLBORONIC ACID;AKOS BRN-0412;4-(TERT-BUTYLDIMETHYLSILYOXY)PHENYLBORON;4-(tert |
IUPAC Name | [4-[tert-butyl(dimethyl)silyl]oxyphenyl]boronic acid |
Molecular Weight | 252.19 g/mol |
Molecular Formula | C12H21BO3Si |
Canonical SMILES | B(C1=CC=C(C=C1)O[Si](C)(C)C(C)(C)C)(O)O |
InChI Key | NVHHEADQQACSCJ-UHFFFAOYSA-N |
Boiling Point | 321.4ºC at 760mmHg |
Melting Point | 194-198ºC(lit.) |
Flash Point | 148.2ºC |
Purity | 98% |
Density | 1.01g/cm³ |
Application | 4-(Tert-Butyl Dimethylsiloxy)Phenyl Boronic Acid serves as a versatile reactant extensively utilized in various chemical syntheses It plays a critical role in asymmetric addition reactions involving β-substituted cyclic enones and facilitates hydroarylation and heterocyclization with phenylpropiolates This compound is integral to double Suzuki-Miyaura coupling reactions providing valuable intermediates for a range of applications Additionally it acts as a starting material in the creation of red electroluminescent polyfluorenes Its utility extends to the synthesis of biologically active molecules including phenylpyridone derivatives functioning as MCH1R antagonists as well as atromentin and its O-alkylated derivatives Furthermore it contributes to the development of inhibitors targeting gelatinases and MT1-MMP underscoring its importance in medicinal chemistry |
Exact Mass | 252.13500 |
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