180516-87-4
Chemical Structure
4-Carboxyphenylboronic acid pinacol ester
- CAS No.: 180516-87-4
- Formula:C13H17BO4
- Molecular Weight:248.09
IUPAC Name: 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid
InChIKey: IYDKBQIEOBXLTP-UHFFFAOYSA-N
SMILES: CC(C(C)(O1)C)(OB1C2=CC=C(C(O)=O)C=C2)C
Biological Activity: 4-Carboxyphenylboronic acid pinacol ester can be used as a starting material for N-(2-acryloylamino-ethyl)-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide (AEBB). 4-Carboxyphenylboronic acid pinacol ester can be used to crosslink epoxidized natural rubber (ENR) to silica. 4-Carboxyphenylboronic acid pinacol ester is a biochemical reagent that can be used as a biological material or organic compound for life science related research[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4-Carboxyphenylboronic acid pinacol ester | 98.0% | 4-Carboxyphenylboronic acid pinacol ester can be used as a starting material for N-(2-acryloylamino-ethyl)-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzamide (AEBB). 4-Carboxyphenylboronic acid pinacol ester can be used to crosslink epoxidized natural rubber (ENR) to silica. 4-Carboxyphenylboronic acid pinacol ester is a biochemical reagent that can be used as a biological material or organic compound for life science related research. | ||||||||||||||||||||
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- [1]. Gertjan Vancoillie, et al., Synthesis and polymerization of boronic acid containing monomers, Polymer Chemistry, Volume 7, Issue 35, 2016, Pages 5484-5495, ISSN 1759-9954.
- [2]. Lingyun Huang, et al., Boronic ester bonds crosslinked vitrimer elastomers with mechanical robustness, shape memory, self-healing and recyclability properties, Composites Science and Technology, Volume 228, 2022, 109621, ISSN 0266-3538.
