4-(tert-Butyldimethylsilyloxy)phenylboronic acid

• Catalog No.: 524042
• CAS Number: 159191-56-7
• M. F.: C12H21BO3Si
• M. W.: 252.18984
• Purity: ≥95%

SYNONYMS

• Title: 4-(叔丁基二甲基硅氧基)苯基硼酸
• IUPAC name: {4-[(tert-butyldimethylsilyl)oxy]phenyl}boronic acid
• IUPAC Traditional name: 4-[(tert-butyldimethylsilyl)oxy]phenylboronic acid
• Synonyms: 4-(tert-Butyldimethylsilyloxy)benzeneboronic acid

DATABASE IDS

• PubChem SID: 24874387
• MDL Number: MFCD03093888
• CAS Number: 159191-56-7

PROPERTIES

• Linear Formula: (CH3)3CSi(CH3)2OC6H4B(OH)2
• Purity: ≥95%
• Melting Point: 194-198 °C(lit.)
• Personal Protective Equipment: Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
• German water hazard class: 3

DETAILS

Description (English)

Packaging
1, 5 g in glass bottle
Application
Reactant involved in:
• Asymmetric addition reactions with β-substituted cyclic enones1
• Hydroarylation and heterocyclization with phenylpropiolates2
• Double Suzuki-Miyaura coupling reactions3Starting material for the synthesis of red electroluminescent polyfluorenes4Reactant involved in the synthesis of biologically active molecules including:
• Phenylpyridone derivatives as MCH1R antagonists5
• Atromentin and its O-alkylated derivatives3
• Gelatinases and MT1-MMP inhibitors6

Description (简体中文)

包装
1, 5 g in glass bottle
Application
Reactant involved in:
• Asymmetric addition reactions with β-substituted cyclic enones1
• Hydroarylation and heterocyclization with phenylpropiolates2
• Double Suzuki-Miyaura coupling reactions3Starting material for the synthesis of red electroluminescent polyfluorenes4Reactant involved in the synthesis of biologically active molecules including:
• Phenylpyridone derivatives as MCH1R antagonists5
• Atromentin and its O-alkylated derivatives3
• Gelatinases and MT1-MMP inhibitors6