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Atomfair 3,5-Dichloro-4-methoxybenzoic acid 2-benzylhydrazide hydrochloride C15H15Cl3N2O2

Description 3,5-Dichloro-4-methoxybenzoic acid 2-benzylhydrazide hydrochloride (CAS No. 403-15-6) is a high-purity organic compound with the molecular formula C15H15Cl3N2O2. This hydrochloride salt derivative features a benzylhydrazide moiety attached to a 3,5-dichloro-4-methoxybenzoic acid scaffold, making it a valuable intermediate for pharmaceutical and agrochemical research. Its IUPAC name is N’-benzyl-3,5-dichloro-4-methoxybenzohydrazide;hydrochloride . The compound is supplied as a crystalline solid with >95% purity (HPLC), ensuring consistency for synthetic applications. Store in a cool, dry place under inert conditions to maintain stability. Suitable for use in coupling reactions, heterocycle synthesis, and as a building block for bioactive molecule development.

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Description

Description

3,5-Dichloro-4-methoxybenzoic acid 2-benzylhydrazide hydrochloride (CAS No. 403-15-6) is a high-purity organic compound with the molecular formula C15H15Cl3N2O2. This hydrochloride salt derivative features a benzylhydrazide moiety attached to a 3,5-dichloro-4-methoxybenzoic acid scaffold, making it a valuable intermediate for pharmaceutical and agrochemical research. Its IUPAC name is N’-benzyl-3,5-dichloro-4-methoxybenzohydrazide;hydrochloride. The compound is supplied as a crystalline solid with >95% purity (HPLC), ensuring consistency for synthetic applications. Store in a cool, dry place under inert conditions to maintain stability. Suitable for use in coupling reactions, heterocycle synthesis, and as a building block for bioactive molecule development.

  • CAS No: 403-15-6
  • Molecular Formula: C15H15Cl3N2O2
  • Molecular Weight: 361.6
  • Exact Mass: 360.019911
  • Monoisotopic Mass: 360.019911
  • IUPAC Name: N’-benzyl-3,5-dichloro-4-methoxybenzohydrazide;hydrochloride
  • SMILES: COC1=C(C=C(C=C1Cl)C(=O)NNCC2=CC=CC=C2)Cl.Cl
  • Synonyms: 23959-69-5, 3,5-Dichloro-4-methoxybenzoic acid 2-benzylhydrazide hydrochloride, DTXSID10946804, Benzoic acid, 3,5-dichloro-4-methoxy-, 2-benzylhydrazide, hydrochloride, N-Benzyl-3,5-dichloro-4-methoxybenzene-1-carbohydrazonic acid–hydrogen chloride (1/1)

Application

This compound serves as a versatile precursor in medicinal chemistry for the synthesis of hydrazide-based inhibitors or receptor modulators. Its dichloro-methoxy substitution pattern enhances electrophilic reactivity, facilitating nucleophilic aromatic substitutions. Researchers utilize it in the development of antimicrobial or antifungal agents due to its potential bioactivity. The benzylhydrazide group allows for further functionalization via reductive amination or condensation reactions.

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