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Ethyl potassium malonate
CAS No. 6148-64-7
Ethyl potassium malonate( Potassium 3-ethoxy-3-oxopropanoate | Malonic Acid Monoethyl Ester Potassium Salt )
Catalog No. M27553 CAS No. 6148-64-7
Ethyl potassium malonate, a competitive inhibitor of the enzyme succinate dehydrogenase, acts as a precursor to produce (trimethylsilyl)ethyl malonate, which is utilized to prepare beta-ketoesters by acylation and serves as an intermediate for the preparation of ethyl tert-butyl malonate.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 10MG | 62 | In Stock |
|
| 25MG | 111 | In Stock |
|
| 100MG | Get Quote | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameEthyl potassium malonate
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NoteResearch use only, not for human use.
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Brief DescriptionEthyl potassium malonate, a competitive inhibitor of the enzyme succinate dehydrogenase, acts as a precursor to produce (trimethylsilyl)ethyl malonate, which is utilized to prepare beta-ketoesters by acylation and serves as an intermediate for the preparation of ethyl tert-butyl malonate.
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DescriptionEthyl potassium malonate, a competitive inhibitor of the enzyme succinate dehydrogenase, acts as a precursor to produce (trimethylsilyl)ethyl malonate, which is utilized to prepare beta-ketoesters by acylation and serves as an intermediate for the preparation of ethyl tert-butyl malonate.
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In Vitro——
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In Vivo——
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SynonymsPotassium 3-ethoxy-3-oxopropanoate | Malonic Acid Monoethyl Ester Potassium Salt
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PathwayOthers
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TargetOther Targets
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RecptormGlu5
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Research Area——
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Indication——
Chemical Information
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CAS Number6148-64-7
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Formula Weight170.205
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Molecular FormulaC5H7KO4
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Purity>98% (HPLC)
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Solubility——
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SMILES[K+].CCOC(=O)CC([O-])=O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Notartomaso S, et al. Expression of the K(+)/Cl(-) cotransporter, KCC2, in cerebellar Purkinje cells is regulated by group-I metabotropic glutamate receptors. Neuropharmacology. 2017 Mar 15;115:51-59.
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