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CAS 6139-83-9

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4-Chlorobutyraldehyde diethyl acetal

Description:
4-Chlorobutyraldehyde diethyl acetal, with the CAS number 6139-83-9, is an organic compound characterized by its acetal functional group, which is formed from the reaction of an aldehyde with an alcohol. This compound features a butyraldehyde backbone substituted with a chlorine atom at the fourth carbon position, contributing to its reactivity and potential applications in organic synthesis. The diethyl acetal structure provides stability and protects the aldehyde group from oxidation, making it useful in various chemical reactions. Typically, it is a colorless to pale yellow liquid with a distinctive odor. The compound is soluble in organic solvents and may have moderate volatility. Its reactivity can be attributed to the presence of the aldehyde moiety, which can participate in nucleophilic addition reactions. Safety precautions should be taken when handling this substance, as it may pose health risks through inhalation or skin contact. Overall, 4-Chlorobutyraldehyde diethyl acetal serves as an important intermediate in the synthesis of more complex organic molecules.
Formula:C8H17ClO2
InChI:InChI=1S/C8H17ClO2/c1-3-10-8(11-4-2)6-5-7-9/h8H,3-7H2,1-2H3
InChI key:InChIKey=JGGRHRMHOUWCDX-UHFFFAOYSA-N
SMILES:C(CCCCl)(OCC)OCC
Synonyms:
  • 4-Chloro Butanal Diethyl Acetal
  • 4-Chloro Butyraldehyde Diethyl Acetal
  • 4-Chloro-1,1-Diethoxy Butane
  • 4-Chloro-1,1-Diethoxybutane
  • 4-Chlorobutanal diethyl acetal
  • Butane, 4-chloro-1,1-diethoxy-
  • Butyraldehyde, 4-chloro-, diethyl acetal
  • NSC 96467
  • γ-Chlorobutyraldehyde diethyl acetal
  • 4-chlorobutyraldehyde diethyl acetal
  • 4-Chlorobutyraldehyde diethyl acetal
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