CAS 141942-85-0
:Ethyl (R)-(-)-4-cyano-3-hydroxybutyrate
Description:
Ethyl (R)-(-)-4-cyano-3-hydroxybutyrate, with the CAS number 141942-85-0, is a chiral compound that belongs to the class of cyano derivatives. It features a cyano group (-C≡N) and a hydroxyl group (-OH) attached to a butyric acid backbone, which contributes to its biological activity. The presence of the ethyl ester group enhances its solubility in organic solvents, making it useful in various chemical reactions and applications. This compound is often utilized in the synthesis of pharmaceuticals and agrochemicals due to its ability to serve as an intermediate in the production of more complex molecules. Its chirality, indicated by the (R)- configuration, is significant in determining its interaction with biological systems, as enantiomers can exhibit different pharmacological effects. Additionally, the compound's stability and reactivity can be influenced by factors such as pH and temperature, which are important considerations in its handling and application in synthetic processes.
Formula:C7H11NO3
InChI:InChI=1/C7H11NO3/c1-2-11-7(10)5-6(9)3-4-8/h6,9H,2-3,5H2,1H3/t6-/m1/s1
InChI key:InChIKey=LOQFROBMBSKWQY-ZCFIWIBFSA-N
SMILES:[C@H](CC(OCC)=O)(CC#N)O
Synonyms:- (3R)-4-cyano-3-hydroxybutyric acid ethyl ester
- (R)-(-)-4-cyano-3-hydroxybutyric acid ethyl ester
- (R)-(-)-ETHYL 4-cyano-3-hydroxybutyrate
- (R)-4-cyano-3-hydrobutyricacid ethyl ester
- (R)-Ethyl 4-cyano-3-hydroxybutanoate
- (S)-4-cyano-3-HYDROXYBUTANOATE ETHYL
- Atorvastatin Calcium Intermediate ATS-5
- Ats-5
- Butanoic acid, 4-cyano-3-hydroxy-, ethyl ester, (3R)-
- Butanoic acid, 4-cyano-3-hydroxy-, ethyl ester, (R)-
- ETHYL (3R)-4-cyano-3-HYDROXY-BUTANOATE
- ETHYL (R)-4-cyano-3-HYDROXYBUTANOATE
- ETHYL (S)-4-cyano-3-HYDROXYBUTANOATE
- Ethyl (R)-(-)-4-cyano-3-hydroxybutyate
- Ethyl (R)-4-cyano-3-hydroxybutyrate
- Ethyl(R)-(-)-4-cyano-3-hydroxybutyrate
- (R)-4-cyano-3-hydroxybutyric
- (R)-4-Cyano-3-hydroxy butanoate
- ETHYL (S)-(+)-4-CYANO-3-HYDROXYBUTYRATE
- (S)-ETHYL-4-CYANO-3-HYDROXYBUTYRATE
- BUTANOIC ACID 4-CYANO-3-HYDROXY-ETHYL ESTER, (S)
- See more synonyms
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Found 10 products.
Ethyl (R)-(-)-4-Cyano-3-hydroxybutyrate
CAS:Formula:C7H11NO3Purity:>97.0%(GC)Color and Shape:Colorless to Light yellow to Light orange clear liquidMolecular weight:157.17Ethyl (R)-(-)-4-cyano-3-hydroxybutyrate, 98%
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C7H11NO3Purity:98%Color and Shape:Clear, colourless to pale yellow, liquidMolecular weight:157.17Butanoic acid, 4-cyano-3-hydroxy-, ethyl ester, (3R)-
CAS:Formula:C7H11NO3Purity:97%Color and Shape:LiquidMolecular weight:157.1671Ethyl (R)-(-)-4-cyano-3-hydroxybutyate
CAS:Ethyl (R)-(-)-4-cyano-3-hydroxybutyatePurity:98%Molecular weight:157.17g/mol(3R)-4-Cyano-3-hydroxybutanoic Acid Ethyl Ester
CAS:Controlled Product<p>Applications (3R)-4-Cyano-3-hydroxybutanoic Acid Ethyl Ester is used in a biocatalytic process for the synthesis of an atorvastatin intermediate and degredation products/impurities.<br>References Ma, S. et al.: Green Chem., 12, 81 (2010); Stach, J. et al.: Coll. Czech. Chem. Comm., 73, 229 (2008);<br></p>Formula:C7H11NO3Color and Shape:NeatMolecular weight:157.17(R)-4-Cyano-3-hydroxy-butyric acid ethyl ester
CAS:Formula:C7H11NO3Purity:97%Color and Shape:LiquidMolecular weight:157.169Ethyl (R)-(-)-4-cyano-3-hydroxybutyrate
CAS:<p>Ethyl (R)-(-)-4-cyano-3-hydroxybutyrate is an asymmetric synthesis of D-(+)-glyceraldehyde. This compound is an acidic, high cholesterol substrate that binds to disaccharides and has hydroxyl groups. It has been shown to reduce low density lipoprotein levels in the blood by inhibiting the production of cholesterol in the liver. The reaction solution is immobilized on a solid support and is used for kinetic studies. Kinetic measurements were performed at different concentrations of hydrochloric acid and immobilized cells as a function of time. The reaction yield was determined using UV absorbance at 275 nm, which was plotted against time.</p>Purity:Min. 95%









