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CAS 36394-75-9

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(S)-(-)-2-Acetoxypropionyl chloride

Description:
(S)-(-)-2-Acetoxypropionyl chloride, with the CAS number 36394-75-9, is an organic compound characterized by its acyl chloride functional group, which makes it reactive and useful in various chemical syntheses. This compound features a chiral center, contributing to its enantiomeric specificity, which is significant in pharmaceutical applications where stereochemistry can influence biological activity. It typically appears as a colorless to pale yellow liquid and has a pungent odor, characteristic of acyl chlorides. The presence of the acetoxy group indicates that it can participate in nucleophilic acyl substitution reactions, making it a valuable intermediate in the synthesis of esters, amides, and other derivatives. Due to its reactivity, it must be handled with care, as it can react violently with water and alcohols, releasing hydrochloric acid. Proper storage in a cool, dry place, away from moisture, is essential to maintain its stability. Overall, (S)-(-)-2-Acetoxypropionyl chloride is an important compound in organic synthesis, particularly in the development of chiral pharmaceuticals.
Formula:C5H7ClO3
InChI:InChI=1S/C5H7ClO3/c1-3(5(6)8)9-4(2)7/h3H,1-2H3/t3-/m0/s1
InChI key:InChIKey=ALHZEIINTQJLOT-VKHMYHEASA-N
SMILES:[C@@H](OC(C)=O)(C(Cl)=O)C
Synonyms:
  • (1R)-2-chloro-2-oxo-1-phenylethyl acetate
  • (1S)-2-chloro-1-methyl-2-oxoethyl acetate
  • (2S)-1-Chloro-1-oxopropan-2-yl acetate
  • (2S)-2-(Acetyloxy)propanoyl chloride
  • (2S)-2-Acetoxypropionyl chloride
  • (S)-1-Chloro-1-oxopropan-2-yl acetate
  • (S)-2-(Acetyloxy)propanoyl chloride
  • (S)-2-Acetoxypropanoyl chloride
  • (S)-2-Acetoxypropionoyl chloride
  • (S)-2-Acetyloxypropionyl chloride
  • See more synonyms
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