K0875
Sodium 2-oxobutyrate
powder
Sinônimo(s):
2-Oxobutanoic acid sodium salt, 2-Oxobutyric acid sodium salt, Sodium α-ketobutyrate
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About This Item
Produtos recomendados
forma
powder
Nível de qualidade
cor
white
temperatura de armazenamento
2-8°C
cadeia de caracteres SMILES
[Na+].CCC(=O)C([O-])=O
InChI
1S/C4H6O3.Na/c1-2-3(5)4(6)7;/h2H2,1H3,(H,6,7);/q;+1/p-1
chave InChI
SUAMAHKUSIHRMR-UHFFFAOYSA-M
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Aplicação
Sodium 2-oxobutyrate can be used in the preparation of metal complexes such as lanthanide poly(imino carboxylate) complexes and half-sandwich complexes of (S)-1-amino-2-(methoxymethyl)-pyrrolidine. It can also be used in the synthesis of antiviral agents, 6-azapyrimidine-2′-deoxy-4′-thionucleosides.
Substrate for the determination of lactate dehydrogenase isoenzymes.
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Half-sandwich complexes of (S)-1-amino-2-(methoxymethyl)-pyrrolidine (SAMP).
Journal of Organometallic Chemistry, 564(1), 179-187 (1998)
Molecular cell, 76(5), 838-851 (2019-10-01)
Intermediary metabolism in cancer cells is regulated by diverse cell-autonomous processes, including signal transduction and gene expression patterns, arising from specific oncogenotypes and cell lineages. Although it is well established that metabolic reprogramming is a hallmark of cancer, we lack
6-Azapyrimidine-2`-deoxy-4`-thionucleosides: Antiviral Agents against TK+ and TK? HSV and VZV Strains.
Journal of Medicinal Chemistry, 47(22), 5482-5491 (2004)
Formation of oligomeric lanthanide complexes with new tripodal poly (imino carboxylate) ligands.
J. Chem. Soc., Dalton Trans., 20, 3655-3658 (1997)
FEMS microbiology letters, 273(1), 70-77 (2007-06-15)
A two-step enzymatic synthesis process of 4-hydroxyisoleucine is suggested. In the first step, the aldol condensation of acetaldehyde and alpha-ketobutyrate catalyzed by specific aldolase results in the formation of 4-hydroxy-3-methyl-2-keto-pentanoate (HMKP). In the second step, amination of HMKP by the
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