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CAS 175135-69-0

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2-(4-Methoxyphenoxy)-5-nitrobenzoyl chloride

Description:
2-(4-Methoxyphenoxy)-5-nitrobenzoyl chloride is an organic compound characterized by its functional groups and structural features. It contains a benzoyl chloride moiety, which is known for its reactivity due to the presence of the acyl chloride functional group. The compound also features a nitro group and a methoxy-substituted phenyl group, contributing to its overall chemical properties and potential reactivity. The presence of the methoxy group can influence the compound's solubility and electronic properties, while the nitro group may enhance its electrophilic character. This compound is typically used in organic synthesis, particularly in the preparation of various derivatives and in the development of pharmaceuticals. Its reactivity allows it to participate in nucleophilic substitution reactions, making it a valuable intermediate in synthetic chemistry. Safety precautions should be taken when handling this compound, as it may be corrosive and harmful if inhaled or ingested. Proper storage and handling in a controlled environment are essential to ensure safety and stability.
Formula:C14H10ClNO5
InChI:InChI=1S/C14H10ClNO5/c1-20-10-3-5-11(6-4-10)21-13-7-2-9(16(18)19)8-12(13)14(15)17/h2-8H,1H3
InChI key:InChIKey=ZHLCCUQAQOFEBB-UHFFFAOYSA-N
SMILES:C(Cl)(=O)C1=C(OC2=CC=C(OC)C=C2)C=CC(N(=O)=O)=C1
Synonyms:
  • 2-(4-Methoxyphenoxy)-5-Nitrobenzoyl Chloride
  • 2-(4-Methoxyphenoxy)-5-nitrobenzene-1-carbonylchloride
  • Benzoyl chloride, 2-(4-methoxyphenoxy)-5-nitro-
  • 2-(4-Methoxyphenoxy)-5-nitrobenzene-1-carbonyl chloride
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