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Atomfair Benzoic acid, 4-(((methylphenylamino)methylene)amino)-, ethyl ester C17H18N2O2

Description Ethyl 4-[(N-methylanilino)methylideneamino]benzoate (CAS: 57834-33-0) is a high-purity organic compound with the molecular formula C17H18N2O2. This benzoate derivative features a unique N-methylanilino and methyleneamino functional group arrangement, making it a valuable intermediate in synthetic organic chemistry and materials science. With a molecular weight of 282.34 g/mol, this compound is supplied as a crystalline solid with >98% purity (HPLC), ensuring consistency for research and industrial applications. Its structure is ideal for studying Schiff base reactivity, coordination chemistry, and photophysical properties. Suitable for use in controlled environments, this product is packaged under inert conditions to guarantee stability and longevity.

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Description

Description

Ethyl 4-[(N-methylanilino)methylideneamino]benzoate (CAS: 57834-33-0) is a high-purity organic compound with the molecular formula C17H18N2O2. This benzoate derivative features a unique N-methylanilino and methyleneamino functional group arrangement, making it a valuable intermediate in synthetic organic chemistry and materials science. With a molecular weight of 282.34 g/mol, this compound is supplied as a crystalline solid with >98% purity (HPLC), ensuring consistency for research and industrial applications. Its structure is ideal for studying Schiff base reactivity, coordination chemistry, and photophysical properties. Suitable for use in controlled environments, this product is packaged under inert conditions to guarantee stability and longevity.

  • CAS No: 57834-33-0
  • Molecular Formula: C17H18N2O2
  • Molecular Weight: 282.34
  • Exact Mass: 282.136827821
  • Monoisotopic Mass: 282.136827821
  • IUPAC Name: ethyl 4-[(N-methylanilino)methylideneamino]benzoate
  • SMILES: CCOC(=O)C1=CC=C(C=C1)N=CN(C)C2=CC=CC=C2
  • Synonyms: 57834-33-0, Ethyl 4-[[(methylphenylamino)methylene]amino]benzoate, Benzoic acid, 4-[[(methylphenylamino)methylene]amino]-, ethyl ester, Ethyl 4-(((methylphenylamino)methylene)amino)benzoate, EINECS 260-976-0

Application

This compound serves as a versatile building block in organic synthesis, particularly for constructing Schiff base ligands in coordination chemistry. Researchers utilize it in the development of photoactive materials due to its conjugated system, which may exhibit unique electronic properties. It is also explored in dye chemistry and as a potential precursor for pharmaceutical intermediates.

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