CAS 86728-85-0
:Butanoic acid, 4-chloro-3-hydroxy-, ethyl ester, (3S)-
Description:
Butanoic acid, 4-chloro-3-hydroxy-, ethyl ester, with the CAS number 86728-85-0, is an organic compound characterized by its ester functional group, which is derived from butanoic acid and contains a chloro and hydroxy substituent. This compound typically exhibits a moderate polarity due to the presence of both the ester and hydroxy groups, influencing its solubility in polar solvents. The chloro substituent can impart unique reactivity, making it useful in various chemical syntheses. The stereochemistry indicated by (3S) suggests a specific three-dimensional arrangement of atoms, which can affect the compound's biological activity and interaction with other molecules. Generally, esters like this one are known for their pleasant odors and are often used in flavoring and fragrance applications. Additionally, the presence of functional groups such as hydroxyl and chloro can enhance its reactivity in organic synthesis, making it a potential candidate for further chemical transformations. Overall, this compound's unique structure and functional groups contribute to its diverse applications in chemistry and related fields.
Formula:C6H11ClO3
InChI:InChI=1S/C6H11ClO3/c1-2-10-6(9)3-5(8)4-7/h5,8H,2-4H2,1H3/t5-/m0/s1
InChI key:InChIKey=ZAJNMXDBJKCCAT-YFKPBYRVSA-N
SMILES:C(C(OCC)=O)[C@@H](CCl)O
Synonyms:- (3S)-4-Chloro-3-hydroxybutyric acid ethyl ester
- (S)-(-)-Ethyl-4-chloro-3-hydroxybutyrate
- (S)-4-Chloro-3-hydroxybutanoic acid ethyl ester
- Ats-4
- Butanoic acid, 4-chloro-3-hydroxy-, ethyl ester, (3S)-
- Butanoic acid, 4-chloro-3-hydroxy-, ethyl ester, (S)-
- Butanoic acid,4-chloro-3-hydroxy-, ethyl ester
- Cobe
- Ethyl (3S)-(-)-4-chloro-3-hydroxybutyrate
- Ethyl (S)-γ-chloro-β-hydroxybutyrate
- Ethyl 4-chloro-3-hydroxybutyrate
- Ethyl S-4-Chloro-3-Hydroxybutyrat
- Ethyl-4-Chloro-4-HydroxyButyrate
- Ethyll-4-Chloro-3-Hydroxy Butyrate
- Ethyl 4-chloro-3-hydroxybutanoate
- S-(-)-Ethyl-4-Chloro-3-Hydroxybutanoate
- ethyl (3R)-4-chloro-3-hydroxybutanoate
- ethyl (3S)-4-chloro-3-hydroxybutanoate
- ethyl (S)-(-)-4-chloro-3-hydroxybutanoate
- Ethyl S-4-chloro-3-hydroxybutyrate
- Ethyl(S)-(-)-4-chloro-3-hydroxybutyrate
- See more synonyms
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Found 8 products.
Ethyl (S)-(-)-4-chloro-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:C6H11ClO3Purity:98%Color and Shape:Clear colorless, LiquidMolecular weight:166.60ETHYL S-4-CHLORO-3-HYDROXYBUTYRATE
CAS:Formula:C6H11ClO3Purity:95%Color and Shape:LiquidMolecular weight:166.6027Ethyl (S)-4-Chloro-3-hydroxybutyrate
CAS:Formula:C6H11ClO3Purity:>95.0%(GC)Color and Shape:Colorless to Light orange to Yellow clear liquidMolecular weight:166.60Ethyl S-4-chloro-3-hydroxybutyrate
CAS:Formula:C6H11ClO3Purity:95%Color and Shape:Liquid, ClearMolecular weight:166.6Ethyl (S)-4-chloro-3-hydroxybutyrate
CAS:Ethyl (S)-4-chloro-3-hydroxybutyratePurity:98%Molecular weight:166.60g/molEthyl (S)-4-chloro-3-hydroxybutyrate
CAS:<p>Ethyl (S)-4-chloro-3-hydroxybutyrate is a chiral compound that is synthesized by asymmetric synthesis. It is an inhibitor of the α subunit of bacterial RNA polymerase, which plays an important role in bacterial growth and replication. This chemical has shown high stability against hydrochloric acid and ethylene diamine, as well as enzyme activities. In addition, the formation rate for fatty acids was increased after treatment with Ethyl (S)-4-chloro-3-hydroxybutyrate.</p>Formula:C6H11ClO3Purity:Min. 95%Molecular weight:166.6 g/mol
