524042
4-(tert-Butyldimethylsilyloxy)phenylboronic acid
≥95%
Synonym(s):
4-(tert-Butyldimethylsilyloxy)benzeneboronic acid
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About This Item
Recommended Products
Assay
≥95%
form
solid
mp
194-198 °C (lit.)
SMILES string
CC(C)(C)[Si](C)(C)Oc1ccc(cc1)B(O)O
InChI
1S/C12H21BO3Si/c1-12(2,3)17(4,5)16-11-8-6-10(7-9-11)13(14)15/h6-9,14-15H,1-5H3
InChI key
NVHHEADQQACSCJ-UHFFFAOYSA-N
Application
Reactant involved in:
Starting material for the synthesis of red electroluminescent polyfluorenes
Reactant involved in the synthesis of biologically active molecules including:
- Asymmetric addition reactions with β-substituted cyclic enones
- Hydroarylation and heterocyclization with phenylpropiolates
- Double Suzuki-Miyaura coupling reactions
Starting material for the synthesis of red electroluminescent polyfluorenes
Reactant involved in the synthesis of biologically active molecules including:
- Phenylpyridone derivatives as MCH1R antagonists
- Atromentin and its O-alkylated derivatives
- Gelatinases and MT1-MMP inhibitors
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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