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CAS 3746-67-6

:

3-(Acetylamino)-4-methoxybenzenesulfonyl chloride

Description:
3-(Acetylamino)-4-methoxybenzenesulfonyl chloride, with the CAS number 3746-67-6, is a chemical compound characterized by its sulfonyl chloride functional group, which is known for its reactivity and utility in organic synthesis. This compound features an acetylamino group and a methoxy group attached to a benzene ring, contributing to its overall chemical properties. The presence of the sulfonyl chloride moiety makes it a potent electrophile, allowing it to participate in nucleophilic substitution reactions, which are valuable in the synthesis of various organic compounds. The acetylamino group enhances its solubility in polar solvents, while the methoxy group can influence its electronic properties and reactivity. This compound is typically used in the synthesis of pharmaceuticals and agrochemicals, where it serves as an intermediate in the formation of more complex molecules. Due to the presence of the sulfonyl chloride, it is important to handle this compound with care, as it can be corrosive and may release toxic gases upon reaction with water or moisture.
Formula:C9H10ClNO4S
InChI:InChI=1S/C9H10ClNO4S/c1-6(12)11-8-5-7(16(10,13)14)3-4-9(8)15-2/h3-5H,1-2H3,(H,11,12)
InChI key:InChIKey=KRKMAUKQDRAOFI-UHFFFAOYSA-N
SMILES:N(C(C)=O)C1=C(OC)C=CC(S(Cl)(=O)=O)=C1
Synonyms:
  • 2-Acetamidoanisole-4-sulfonyl chloride
  • 3-(Acetylamino)-4-methoxybenzenesulfonyl chloride
  • 3-Acetamido-4-methoxybenzene-1-sulfonyl chloride
  • 3-Acetamido-4-methoxybenzene-1-sulfonylchloride
  • 3-Acetamido-4-methoxybenzenesulfonyl chloride
  • Benzenesulfonyl chloride, 3-(acetylamino)-4-methoxy-
  • Metanilyl chloride, N-acetyl-4-methoxy-
  • N-Acetyl-4-methoxymetanilyl chloride
  • 3-Acetamido-4-methoxybenzenesulphonyl chloride
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