CAS 22987-21-9
:Ácido 2-hidroxietanofosfônico
- 2-Hydroxyethanephosphonic acid
- 2-Hydroxyethephon
- Brn 1751212
- Ethephon-hydroxy
- Hydroxyethephon
- P-(2-Hydroxyethyl)phosphonic acid
- Phosphonic acid, (2-hydroxyethyl)-
- Phosphonic acid, P-(2-hydroxyethyl)-
- (2-Hydroxyethyl)phosphonic acid
- (2-Hydroxyethyl)phosphonic acid
Phosphonic acid, P-(2-hydroxyethyl)-
CAS:Fórmula:C2H7O4PPureza:95%Cor e Forma:SolidPeso molecular:126.0483(2-Hydroxyethyl)phosphonic acid
CAS:(2-Hydroxyethyl)phosphonic acidPureza:95% (contains <6%solvent)Peso molecular:126.05g/molEthephon-hydroxy 100 µg/mL in Acetonitrile
CAS:Fórmula:C2H7O4PCor e Forma:ColourlessPeso molecular:126.052-Hydroxyethanephosphonic Acid
CAS:Stability Hygroscopic
Applications 2-Hydroxyethanephosphonic acid is an substrate used in the study of 2-hydroxyethylphosphonate dioxygenase reaction mechanism. 2-Hydroxyethanephosphonic Acid is also a required intermediate in labelled Fosfomycin (F727502) biosynthesis.
References Hirao, H., et al.: J. Am. Chem. Soc., 133, 14550 (2011); Hidaka, T., et al.: J. Antibiot., 45, 1008 (1992); Patel, S., et al.: Drugs, 53, 637 (1997); Ribes, S., et al.: J. Antimicrob. Chemother., 57, 931 (2006);Fórmula:C2H7O4PCor e Forma:Colourless To RedPeso molecular:126.052-Hydroxyethanephosphonic Acid-d4
CAS:Produto ControladoApplications 2-Hydroxyethanephosphonic acid is an substrate used in the study of 2-hydroxyethylphosphonate dioxygenase reaction mechanism. 2-Hydroxyethanephosphonic Acid is also a required intermediate in labelled Fosfomycin (F727502) biosynthesis.
References Hirao, H., et al.: J. Am. Chem. Soc., 133, 14550 (2011); Hidaka, T., et al.: J. Antibiot., 45, 1008 (1992); Patel, S., et al.: Drugs, 53, 637 (1997); Ribes, S., et al.: J. Antimicrob. Chemother., 57, 931 (2006)Fórmula:C2H3D4O4PCor e Forma:Light YellowPeso molecular:130.072-Hydroxyethylphosphonic acid
CAS:2-Hydroxyethylphosphonic acid (2-HEP) is a bifunctional reagent that reacts with hexadecanoic acid (16:0) to form 2-hydroxyethylhexadecanoic acid (2-HEHA). This reaction is catalyzed by the enzyme pyridoxal phosphate, which acts as a cofactor. The carbonyl group of 2-HEP reacts with the hydroxyl group of 2-HEHA to form an ester linkage, which can be cleaved by bond cleavage because it is a carboxylic acid. This process is used in analytical chemistry and has been shown to improve the quality of transgenic crops and chemical structures. The crystal structure of 2-HEP was obtained using x-ray diffraction and showed that the molecule has a flat shape with two hydroxyl groups at opposite ends.
Fórmula:C2H7O4PPureza:Min. 95%Peso molecular:126.05 g/mol







