Molecular Formula | C11H10FeO10* |
Molar Mass | 214.04 |
Density | 1.149g/cm3 |
Melting Point | 118-120 °C (lit.) |
Boling Point | 144.7°C at 760 mmHg |
Flash Point | 41.2°C |
Water Solubility | INSOLUBLE |
Vapor Presure | 5.03mmHg at 25°C |
Appearance | Crystallization |
Color | Orange to red to brown |
Exposure Limit | ACGIH: TWA 1 mg/m3NIOSH: TWA 1 mg/m3 |
Maximum wavelength(λmax) | ['314nm(DMF aq.)(lit.)'] |
Storage Condition | Keep in dark place,Sealed in dry,Room Temperature |
Stability | Stable. Incompatible with strong oxidizing agents. |
Sensitive | Air Sensitive |
Refractive Index | 1.623 |
MDL | MFCD00001429 |
Physical and Chemical Properties | Melting point 118-120°C(lit.) water-soluble INSOLUBLE |
Safety Description | S22 - Do not breathe dust. S24/25 - Avoid contact with skin and eyes. |
WGK Germany | 3 |
TSCA | Yes |
HS Code | 29319090 |
EPA chemical information | Information provided by: ofmpub.epa.gov (external link) |
Use | Used to prepare chiral ethylene imino methanol ferrocene, used in the selective azomethine ylide cyclization addition reaction for the preparation of chiral ethylene imino methanol ferrocene, used in the selective azomethine ylide cyclization addition reaction for photosensitizers, preservatives, chiral catalysts and intermediates of anti-tumor medicine (aircraft stealth raw materials). Used to prepare chiral ethylene imino methanol ferrocene, applied to selective azomethine ylide cyclization addition reaction |
application | ferrocene formaldehyde can be used to synthesize various ferrocene derivatives, such as ferrocene Schiff base. |
Preparation | Ferrocene formaldehyde can be obtained by reacting ferrocene and N-methylformanilide in phosphorus oxychloride and treating with sodium bicarbonate. N,N-dimethylformamide is used to participate in the reaction, and the product can be obtained through similar steps. |