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Atomfair 4-Chloro-N-methoxy-N-methylbenzamide C9H10ClNO2

Description 4-Chloro-N-methoxy-N-methylbenzamide (CAS No. 122334-37-6) is a high-purity organic compound with the molecular formula C9H10ClNO2. This specialized benzamide derivative is widely utilized in pharmaceutical and agrochemical research due to its versatile reactivity as an intermediate. The compound features a chloro-substituted benzene ring coupled with a methoxy-methyl amide functional group, offering unique electronic and steric properties for synthetic applications. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a white to off-white crystalline powder under inert packaging to maintain stability. Ideal for nucleophilic substitution reactions, cross-coupling methodologies, and medicinal chemistry projects. Available in research quantities from…

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Description

Description

4-Chloro-N-methoxy-N-methylbenzamide (CAS No. 122334-37-6) is a high-purity organic compound with the molecular formula C9H10ClNO2. This specialized benzamide derivative is widely utilized in pharmaceutical and agrochemical research due to its versatile reactivity as an intermediate. The compound features a chloro-substituted benzene ring coupled with a methoxy-methyl amide functional group, offering unique electronic and steric properties for synthetic applications. Our product is rigorously tested to ensure ??98% purity (HPLC) and is supplied as a white to off-white crystalline powder under inert packaging to maintain stability. Ideal for nucleophilic substitution reactions, cross-coupling methodologies, and medicinal chemistry projects. Available in research quantities from 100mg to 10kg with optional COA and NMR spectra upon request.

  • CAS No: 122334-37-6
  • Molecular Formula: C9H10ClNO2
  • Molecular Weight: 199.63
  • Exact Mass: 199.0400063
  • Monoisotopic Mass: 199.0400063
  • IUPAC Name: 4-chloro-N-methoxy-N-methylbenzamide
  • SMILES: CN(C(=O)C1=CC=C(C=C1)Cl)OC
  • Synonyms: 4-CHLORO-N-METHOXY-N-METHYLBENZAMIDE, 122334-37-6, DTXSID40460861, DTXCID30411680, 833-594-2

Application

4-Chloro-N-methoxy-N-methylbenzamide serves as a key building block in the synthesis of Weinreb amides for ketone formation via Grignard reactions. It is employed in pharmaceutical research for developing protease inhibitors and kinase modulators due to its stable amide bond. The chloro substituent enables further functionalization through palladium-catalyzed cross-coupling reactions in drug discovery pipelines.

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