15991-13-6
15991-13-6
Chemical Structure
Methyl 2-(7-hydroxy-2-oxo-2H-chromen-4-yl)acetate
- CAS No.: 15991-13-6
- Formula:C12H10O5
- Molecular Weight:234.20
IUPAC Name: methyl 2-(7-hydroxy-2-oxo-2H-chromen-4-yl)acetate
InChIKey: YRNMDWOVAZLMDY-UHFFFAOYSA-N
SMILES: O=C1OC(C=C(O)C=C2)=C2C(CC(OC)=O)=C1
Biological Activity: Methyl 2-(7-hydroxy-2-oxo-2H-chromen-4-yl)acetate, a natural coumarins derivative, is exploited for the synthesis of the switchable fluorescent substrates to be used in bacterial enzyme detection[1][2][3].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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Methyl 2-(7-hydroxy-2-oxo-2H-chromen-4-yl)acetate | 97.39% | Methyl 2-(7-hydroxy-2-oxo-2H-chromen-4-yl)acetate, a natural coumarins derivative, is exploited for the synthesis of the switchable fluorescent substrates to be used in bacterial enzyme detection. | ||||||||||||||||||||
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References
- [1]. Nascimento JSD, et al. Mapping the Biotransformation of Coumarins through Filamentous Fungi. Molecules. 2019 Sep 29;24(19). [Content Brief]
- [2]. Lizzul-Jurse A, et al. Readily functionalizable phosphonium-tagged fluorescent coumarins for enhanced detection of conjugates by mass spectrometry. Org Biomol Chem. 2016 Aug 10;14(32):7777-91. [Content Brief]
- [3]. Giovannini G, et al. Coumarin-based, switchable fluorescent substrates for enzymatic bacterial detection. Talanta. 2018 Oct 1;188:448-453. [Content Brief]
