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CAS 56077-78-2

:

Acetic acid, 2-[4-(chlorosulfonyl)phenoxy]-, methyl ester

Description:
Acetic acid, 2-[4-(chlorosulfonyl)phenoxy]-, methyl ester, with the CAS number 56077-78-2, is an organic compound characterized by its ester functional group derived from acetic acid and a phenoxy group substituted with a chlorosulfonyl moiety. This compound typically appears as a colorless to pale yellow liquid and is soluble in organic solvents. It exhibits properties associated with both acetic acid and sulfonyl chlorides, making it reactive towards nucleophiles. The presence of the chlorosulfonyl group enhances its electrophilic character, allowing it to participate in various chemical reactions, including nucleophilic substitution and coupling reactions. This compound is often used in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Due to its reactive nature, it should be handled with care, as it may pose hazards such as irritation to skin and eyes, and it may release toxic fumes upon decomposition. Proper safety protocols should be followed when working with this substance in a laboratory setting.
Formula:C9H9ClO5S
InChI:InChI=1S/C9H9ClO5S/c1-14-9(11)6-15-7-2-4-8(5-3-7)16(10,12)13/h2-5H,6H2,1H3
InChI key:InChIKey=ISHZBFTYSQSGBF-UHFFFAOYSA-N
SMILES:S(Cl)(=O)(=O)C1=CC=C(OCC(OC)=O)C=C1
Synonyms:
  • (4-Chlorosulfonylphenoxy)acetic acid methyl ester
  • Acetic acid, 2-[4-(chlorosulfonyl)phenoxy]-, methyl ester
  • Acetic acid, [4-(chlorosulfonyl)phenoxy]-, methyl ester
  • Acetic acid, [p-(chlorosulfonyl)phenoxy]-, methyl ester
  • Methyl (4-chlorosulfonylphenoxy)acetate
  • Methyl [4-(Chlorosulfonyl)Phenoxy]Acetate
  • Methyl 2-(4-(Chlorosulfonyl)Phenoxy)Acetate
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