Description
tert-Butyl (4-vinylphenyl) carbonate (CAS No. 87188-51-0) is a high-purity specialty chemical with the molecular formula C13H16O3, widely utilized in advanced organic synthesis and polymer research. This compound, also known as TBSM, features a reactive vinyl group and a tert-butyl carbonate moiety, making it a versatile building block for controlled polymerization, surface modification, and functional material development. Its stability under various reaction conditions ensures reliable performance in both academic and industrial applications. Packaged under inert gas to maintain integrity, this product is ideal for researchers requiring precise and reproducible results in photoresist chemistry, click chemistry, and macromolecular engineering.
Properties
- CAS Number: 87188-51-0
- Complexity: 244
- IUPAC Name: tert-butyl (4-vinylphenyl) carbonate
- InChI: InChI=1S/C13H16O3/c1-5-10-6-8-11(9-7-10)15-12(14)16-13(2,3)4/h5-9H,1H2,2-4H3
- InChI Key: GJWMYLFHBXEWNZ-UHFFFAOYSA-N
- Exact Mass: 220.109944368
- Molecular Formula: C13H16O3
- Molecular Weight: 220.26
- SMILES: CC(C)(C)OC(=O)OC1=CC=C(C=C1)C=C
- Topological: 35.5
- Monoisotopic Mass: 220.109944368
- Synonyms: 87188-51-0, Carbonic acid, 1,1-dimethylethyl 4-ethenylphenyl ester, tert-Butyl 4-vinylphenyl carbonate, TBSM, tert-Butyl (4-vinylphenyl) carbonate, p-tert-butoxycarbonyloxystyrene, tert-butyl (4-ethenylphenyl) carbonate, 4-t-butoxycarbonyloxystyrene, 4-BOC-styrene, tert-butyl 4-ethenylphenyl carbonate, p-tert-Butoxycarbonyloxystyrene monomer, TERT-BUTYL4-VINYLPHENYLCARBONATE, 1,1-Dimethylethyl 4-ethenylphenyl carbonate, C-1566, MFCD00145182, p-t-butoxycarbonyloxystyrene, p-tertbutoxycarbonyloxystyrene, SCHEMBL220773, 4-(t-butoxycarbonyloxy)styrene, SCHEMBL6606984, 4-tert-butyloxycarbonyloxystyrene, DTXSID2073695, 4-(t-butyloxycarbonyloxy)styrene, 4-tertiarybutoxycarbonyloxystyrene, 4-(tert-butoxycarbonyloxy)styrene, 4-tertiary-butoxycarbonyloxystyrene, BS-49263, DB-166619, 1,1-Dimethylethyloxycarbonic acid 4-ethenylphenyl ester
Application
tert-Butyl (4-vinylphenyl) carbonate serves as a key monomer in the synthesis of advanced polymers with tailored properties, such as stimuli-responsive hydrogels or photopatternable resins. It is also employed in surface-initiated polymerization to create functional coatings for biomedical devices. Researchers leverage its vinyl group for thiol-ene reactions in bioconjugation and material crosslinking.
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