N-(4-Methoxybenzylidene)aniline
>98.0%(GC)(T)
- Product Code: 94347
CAS:
836-41-9
| Molecular Weight: | 211.26 g./mol | Molecular Formula: | C₁₄H₁₃NO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00025836 | |
| Melting Point: | 63°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of various fine chemicals and pharmaceuticals. Its structure, featuring both an aniline and a methoxybenzylidene group, makes it suitable for use in the development of Schiff base ligands, which are crucial in coordination chemistry for forming complexes with metal ions. These complexes are often explored for their potential in catalysis, material science, and biological applications. Additionally, it may be employed in the synthesis of dyes and pigments due to its aromatic and conjugated system, which can impart color and stability to the resulting products. In research, it serves as a model compound for studying photophysical properties and reaction mechanisms involving imine formation and transformations.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Light red to Green powder to crystal |
| PURITYGC | 98 100% |
| PurityNonaqueous Titration | 98 100% |
| Infrared spectrum | Conforms to Structure |
| SOLUBILITY IN METHANOL | almost transparency |
| MELTING POINT | 61-67 |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | £17.87 |
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| 5.000 | 10-20 days | £57.67 |
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| 25.000 | 10-20 days | £191.34 |
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N-(4-Methoxybenzylidene)aniline
This compound is primarily utilized in organic synthesis as an intermediate for the preparation of various fine chemicals and pharmaceuticals. Its structure, featuring both an aniline and a methoxybenzylidene group, makes it suitable for use in the development of Schiff base ligands, which are crucial in coordination chemistry for forming complexes with metal ions. These complexes are often explored for their potential in catalysis, material science, and biological applications. Additionally, it may be employed in the synthesis of dyes and pigments due to its aromatic and conjugated system, which can impart color and stability to the resulting products. In research, it serves as a model compound for studying photophysical properties and reaction mechanisms involving imine formation and transformations.
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