14047-29-1
14047-29-1
Chemical Structure
4-Boronobenzoic acid
- CAS No.: 14047-29-1
- Formula:C7H7BO4
- Molecular Weight:165.94
IUPAC Name: 4-boronobenzoic acid
InChIKey: SIAVMDKGVRXFAX-UHFFFAOYSA-N
SMILES: O=C(C1=CC=C(B(O)O)C=C1)O
Biological Activity: 4-Boronobenzoic acid is an organic compound. 4-Boronobenzoic acid forms reversible cyclic boronate esters with molecules containing cis-vicinal diol structures (such as sialic acid) through the boron atom, achieving molecular recognition and binding. 4-Boronobenzoic acid can be used in research of breast cancer [1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4-Boronobenzoic acid | 99.81% | 4-Boronobenzoic acid is an organic compound. 4-Boronobenzoic acid forms reversible cyclic boronate esters with molecules containing cis-vicinal diol structures (such as sialic acid) through the boron atom, achieving molecular recognition and binding. 4-Boronobenzoic acid can be used in research of breast cancer . | ||||||||||||||||||||
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References
- [1]. Daze KD, et al. Synthesis of new trisulfonated calix[4]arenes functionalized at the upper rim, and their complexation with the trimethyllysine epigenetic mark. Org Lett. 2012 Mar 16;14(6):1512-5. [Content Brief]
- [2]. Li F, et al. Spatiotemporally programmable cascade hybridization of hairpin DNA in polymeric nanoframework for precise siRNA delivery. Nat Commun. 2021 Feb 18;12(1):1138. [Content Brief]
