CAS 90866-33-4
:(R)-(+)-ethyl-4-chloro-3-hydroxybutanoate
Description:
(R)-(+)-ethyl-4-chloro-3-hydroxybutanoate is an organic compound characterized by its chiral nature, which is indicated by the (R)- configuration. This compound features a chloro substituent at the fourth carbon and a hydroxy group at the third carbon of a butanoate chain, contributing to its reactivity and potential applications in synthesis. It is an ester, derived from the reaction of a carboxylic acid and an alcohol, specifically ethyl alcohol in this case. The presence of the hydroxy group suggests it may participate in hydrogen bonding, influencing its solubility and boiling point. The chloro group can also serve as a site for nucleophilic substitution reactions, making it a valuable intermediate in organic synthesis. This compound is typically used in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. Its specific stereochemistry can affect the biological activity and interaction with other molecules, making it important in chiral synthesis and drug design.
Formula:C6H11ClO3
InChI:InChI=1/C6H11ClO3/c1-2-10-6(9)3-5(8)4-7/h5,8H,2-4H2,1H3
SMILES:CCOC(=O)CC(CCl)O
Synonyms:- Ethyl (R)-(+)-4-chloro-3-hydroxybutyrate
- (R)-(+)-4-Chloro-
- 3-hydroxybutyric acid ethyl ester
- (R)-4-chloro-3-hydroxybutyric acid ethyl ester
- (R)-4-Chloro-3-hydroxybutanoic acid ethyl ester
- Ethyl (R)-4-chloro-3-Hydroxybutanoate
- butanoic acid, 4-chloro-3-hydroxy-, Ethyl ESTER,(R)
- 4-Chloro-3-hydroxybutyric acid ethyl ester
- (R)-(+)-Ethyl-4-chloro-3-hydroxybutyrate
- Ethyl(R)-(+)-4-chloro-3-hydroxy butyrate
- R(+)-Ethyl-4-Chloro-3-Hydroxybutanoate
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Found 9 products.
Ethyl (R)-(+)-4-chloro-3-hydroxybutyrate, 97%, ee 96%
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:C6H11ClO3Purity:96%Color and Shape:Clear colorless, LiquidMolecular weight:166.60Ethyl (R)-(+)-4-Chloro-3-Hydroxybutyrate
CAS:Formula:C6H11ClO3Purity:97%Color and Shape:LiquidMolecular weight:166.6027Ethyl (R)-(+)-4-chloro-3-hydroxybutyrate
CAS:Ethyl (R)-(+)-4-chloro-3-hydroxybutyratePurity:98%Molecular weight:166.60g/molEthyl (R)-4-Chloro-3-hydroxybutanoate
CAS:Formula:C6H11ClO3Purity:>97.0%(GC)Color and Shape:Colorless to Light yellow clear liquidMolecular weight:166.60(R)-Ethyl 4-chloro-3-hydroxybutanoate
CAS:Formula:C6H11ClO3Purity:95%Color and Shape:LiquidMolecular weight:166.6(R)-Ethyl 4-Chloro-3-hydroxybutanoate (~90%)
CAS:Controlled Product<p>Applications (R)-Ethyl 4-chloro-3-hydroxybutanoate is used in biological studies for asymmetric reduction of ethyl 4-chloro-3-oxobutanoate to ethyl (R)-4-chloro-3-hydroxybutanoate with two co-existing, recombinant Escherichia coli strains.<br>References Liu, Y., et al.: Biotech. Lett., 27, 119 (2005);<br></p>Formula:C6H11ClO3Purity:~90%Color and Shape:NeatMolecular weight:166.6Ethyl (R)-(+)-4-chloro-3-hydroxybutyrate
CAS:<p>Ethyl (R)-(+)-4-chloro-3-hydroxybutyrate is a chiral compound with two stereoisomers, one of which is the natural form. It can be synthesized by asymmetric synthesis from ethylene diamine and acetaldehyde. This reaction is catalysed by enzymes such as dehydrogenase, which are used in the biosynthesis of other compounds. The enzyme catalysis results in a high activation energy. Ethyl (R)-(+)-4-chloro-3-hydroxybutyrate also has an organic solvent that is required for its synthesis, d-xylose. The enzyme expression plasmid that is used to express this compound requires recombinant cells.</p>Formula:C6H11ClO3Purity:Min. 95%Color and Shape:Clear LiquidMolecular weight:166.6 g/mol








