| Weight | 176.259 g/mol |
|---|---|
| Formula | C12H16O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
4-tert-Butoxystyrene (95418-58-9)
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- The synthesis, characterization, and deblocking of poly(4-tert-butoxystyrene) and poly(4-tert-butoxy-.alpha.-methylstyrene) (Macromolecules, 1989)
- Living cationic polymerization of 4tertbutoxystyrene and synthesis of poly(4vinylphenol) with narrow molecular weight distribution (Macromolecular Chemistry and Physics, 1989)
- Photolysis-induced micellization of a poly(4-tert-butoxystyrene)-block-polystyrene diblock copolymer (Colloid and Polymer Science, 2008)
- Monomer sequence of partially hydrolyzed poly(4-tert-butoxystyrene) and morphology of diblock copolymers composing this polymer sequence as one block (Polymer, 2011)
- Microphase-Separated Structures of Poly(4-tert-butylstyrene-block-4-tert-butoxystyrene) upon Gradual Changes in Segregation Strength through Hydrolysis Reaction (Macromolecules, 2011)
- Living Cationic Sequential Block Copolymerization of Isobutylene with 4tertButoxystyrene: Synthesis and Characterization of Poly(phydroxystyrenebisobutylenebphydroxystyrene) Triblock Copolymers (Journal of Macromolecular Science, Part A, 2007)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESCC(C)(C)OC1=CC=C(C=C1)C=C
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InChIKeyGRFNSWBVXHLTCI-UHFFFAOYSA-N
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Synthesis
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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methyl 2-(4-isopropoxyphenyl)acetate
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AC1LTEQK
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4-tert-Butoxystyrene
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