Introduction：Basic information about FERROCENEACETIC ACID CAS 1287-16-7, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
FERROCENEACETIC ACID Basic information
| Product Name: | FERROCENEACETIC ACID |
| Synonyms: | Ferrocenylacetic acid, min. 98%;Ferroceneacetic acid,98%;Ferrocenylacetic acid ,97%;Ferroceneacetic acid 98%;Ferroceneacetic acid, 98% 1GR;NSC 128978;ferroceneacetic;Carboxymethylferrocene |
| CAS: | 1287-16-7 |
| MF: | C12H12FeO2 |
| MW: | 244.07 |
| EINECS: | |
| Product Categories: | metallocene;Electrochemical Detection (HPLC Labeling Reagents);Fe (Iron) Compounds;Ferrocenes;HPLC Labeling Reagents;Metallocenes;Transition Metal Compounds;Catalysis and Inorganic Chemistry;Chemical Synthesis;Acetics acid and esters;Analytical Chemistry;Classes of Metal Compounds |
| Mol File: | 1287-16-7.mol |
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FERROCENEACETIC ACID Chemical Properties
| Melting point | 158-160 °C(lit.) |
| storage temp. | Inert atmosphere,Room Temperature |
| solubility | DMSO (Slightly), Methanol (Slightly) |
| form | Crystalline Powder |
| color | Gold to orange-brown |
| Stability: | Stable. Incompatible with strong oxidizing agents. |
Safety Information
| Hazard Codes | Xn |
| Risk Statements | 36/37/38-22 |
| Safety Statements | 37/39-26 |
| WGK Germany | 3 |
| HS Code | 29319090 |
FERROCENEACETIC ACID Usage And Synthesis
| Chemical Properties | gold powder |
| Uses | Ferroceneacetic acid is a versatile catalyst. Also used in the preparation of silver nanoparticles as well as in the synthesis of redox-triggered drug delivery vesicles for cancer cell treatment. |
| Synthesis | 1271-55-2 1287-16-7 The general procedure for the synthesis of ferrocene acetic acid from acetylferrocene was as follows: 0.01 mol of acetylferrocene, 0.1 mol of morpholine, 0.05 mol of sulfur powder, and 0.001 mol of Na2S-9H2O were sequentially added to a 500 mL three-necked flask equipped with a mechanical stirrer and a spherical condenser, and the system was heated in an oil bath to 128 °C, and the reaction was maintained at reflux for 7 h, during which the reaction was monitored by thin-layer chromatography (TLC). for 7 h, during which the reaction progress was monitored by thin layer chromatography (TLC). Upon completion of the reaction, the mixture was cooled to room temperature, followed by the addition of 10 mL of ethanol and 25 mL of 2 mol/L aqueous sodium hydroxide solution, stirred and heated to reflux for 4 h. The reaction continued to be monitored by TLC. After the reaction was complete, the reaction mixture was cooled, the pH was adjusted to 7-8 with dilute hydrochloric acid, and the precipitate was filtered and washed. Subsequently, the pH of the filtrate was adjusted to 1 with hydrochloric acid, left overnight, the precipitate was collected by filtration and washed to give the yellow-brown solid product ferrocene acetic acid in 79% yield. |
| References | [1] Patent: CN104231004, 2017, B. Location in patent: Paragraph 0033; 0042; 0051; 0060; 0069
[2] Angewandte Chemie - International Edition in English, 1997, vol. 36, # 22, p. 2456 - 2458 |
FERROCENEACETIC ACID Preparation Products And Raw materials
| Raw materials | Water-->Acetylferrocene-->Sodium hydroxide-->Ethanol |
