4H-1-Benzopyran-4-one, 3-(2,4-dimethoxyphenyl)-2,3-dihydro-5,7-dihydroxy-
Homoferreirin
CAS: 482-01-9
Molecular Formula: C17H16O6
4H-1-Benzopyran-4-one, 3-(2,4-dimethoxyphenyl)-2,3-dihydro-5,7-dihydroxy- - Names and Identifiers
| Name | Homoferreirin |
| Synonyms | Homoferreirin 5,7-Dihydroxy-2',4'-dimethoxy-isoflavanon 5,7-Dihydroxy-2',4'-dimethoxyisoflavanone 2,3-Dihydro-5,7-dihydroxy-2',4'-dimethoxyisoflavone 3-(2,4-dimethoxyphenyl)-5,7-dihydroxy-chroman-4-one 4H-1-Benzopyran-4-one, 3-(2,4-dimethoxyphenyl)-2,3-dihydro-5,7-dihydroxy- |
| CAS | 482-01-9 |
4H-1-Benzopyran-4-one, 3-(2,4-dimethoxyphenyl)-2,3-dihydro-5,7-dihydroxy- - Physico-chemical Properties
| Molecular Formula | C17H16O6 |
| Molar Mass | 316.31 |
| Melting Point | 168-169℃ |
| Storage Condition | 2-8℃ |
4H-1-Benzopyran-4-one, 3-(2,4-dimethoxyphenyl)-2,3-dihydro-5,7-dihydroxy- - Introduction
Homoferreirin(Homoferreirin) is an organic iron compound with the chemical formula Fe(CO)4(C6H4Me)2. It is a reddish-brown solid, soluble in organic solvents such as benzene and toluene.
Homoferreirin has many application prospects. First, it can function as a catalyst in organic synthesis. The coordination of the iron atom can react with the reactants to promote the chemical reaction, and has high efficiency and selectivity. Secondly, Homoferreirin can be used as an electrochemical infrared material for the preparation of various electrochemical devices and optical sensors. In addition, it can also be used to synthesize other organometallic complexes and expand the research field of synthetic chemistry.
A common method for preparing Homoferreirin is to replace electron-deficient iron carbene with carbon-based ligands. This process is typically carried out in a conductive solvent, such as diethyl ether or tetrahydrofuran, and at low temperatures. The synthesis process requires careful handling due to the high reactivity of the iron carbene, while care is taken to prevent ignition and skin contact during the operation.
Regarding the safety information of Homoferreirin, it is an organometallic compound with certain toxicity. Contact or inhalation of its powder or solution may cause irritation to the skin, eyes and respiratory system. Therefore, appropriate protective measures such as goggles, gloves and dust masks should be worn when handling Homoferreirin. If you accidentally ingest or come into contact with Homoferreirin, you should seek medical attention immediately.
Homoferreirin has many application prospects. First, it can function as a catalyst in organic synthesis. The coordination of the iron atom can react with the reactants to promote the chemical reaction, and has high efficiency and selectivity. Secondly, Homoferreirin can be used as an electrochemical infrared material for the preparation of various electrochemical devices and optical sensors. In addition, it can also be used to synthesize other organometallic complexes and expand the research field of synthetic chemistry.
A common method for preparing Homoferreirin is to replace electron-deficient iron carbene with carbon-based ligands. This process is typically carried out in a conductive solvent, such as diethyl ether or tetrahydrofuran, and at low temperatures. The synthesis process requires careful handling due to the high reactivity of the iron carbene, while care is taken to prevent ignition and skin contact during the operation.
Regarding the safety information of Homoferreirin, it is an organometallic compound with certain toxicity. Contact or inhalation of its powder or solution may cause irritation to the skin, eyes and respiratory system. Therefore, appropriate protective measures such as goggles, gloves and dust masks should be worn when handling Homoferreirin. If you accidentally ingest or come into contact with Homoferreirin, you should seek medical attention immediately.
Last Update：2024-04-10 22:29:15
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CAS: 482-01-9
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CAS: 482-01-9
Tel: 18301782025
Email: 3008007409@qq.com
Mobile: 18021002903
QQ: 3008007409
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