(ethyl 4-chloro-3-ethoxy-3-hydroxybutyrato)iodomagnesium
(ethyl 4-chloro-3-ethoxy-3-hydroxybutyrato)iodomagnesium
CAS: 66161-48-6
Molecular Formula: C8H14ClIMgO4
(ethyl 4-chloro-3-ethoxy-3-hydroxybutyrato)iodomagnesium - Names and Identifiers
| Name | (ethyl 4-chloro-3-ethoxy-3-hydroxybutyrato)iodomagnesium |
| Synonyms | (ethyl 4-chloro-3-ethoxy-3-hydroxybutyrato)iodomagnesium |
| CAS | 66161-48-6 |
| EINECS | 266-185-7 |
(ethyl 4-chloro-3-ethoxy-3-hydroxybutyrato)iodomagnesium - Physico-chemical Properties
| Molecular Formula | C8H14ClIMgO4 |
| Molar Mass | 360.85683 |
(ethyl 4-chloro-3-ethoxy-3-hydroxybutyrato)iodomagnesium - Introduction
(Acetobarterol ester) magnesium iodide is an organic compound with the molecular formula C8H15ClIO3Mg. The following is a description of its nature, use, preparation and safety information:
properties: (acetyl barterol ester) magnesium iodide is a colorless or pale yellow solid. It has good solubility, can be easily dissolved in organic solvents, and is stable. Its chemical properties make it widely used in organic synthesis.
Uses: (Acetyl Barterol Ester) Magnesium iodide is commonly used in the field of organic synthesis, especially alkyl, alkynyl or alkenylation reactions initiated by lithium or magnesium reagents. It can be used as an effective Grignard reagent to react with halogenated hydrocarbons or aldehyde ketals to form the corresponding alkyl, alkynyl or alkenyl magnesium reagents.
Preparation Method: (Acetobarterol Ester) Magnesium iodide is usually prepared by adding an acetic acid esterifying agent, benzidine and magnesium iodide to an acetone solution. This process can be carried out at room temperature and can be completed within a few hours.
Safety Information: (Acetobarterol Ester) Magnesium Iodide is relatively non-hazardous in general. However, as a safe handling principle for all chemical substances, appropriate laboratory precautions, including wearing protective glasses and gloves, must be used to avoid inhalation, ingestion or contact. In addition, the substance should be evaluated for safety according to the conditions and use of the specific synthesis reaction to ensure safe use in laboratory and industrial environments. In all cases, the safety data sheet and operating instructions for the substance should be reviewed.
properties: (acetyl barterol ester) magnesium iodide is a colorless or pale yellow solid. It has good solubility, can be easily dissolved in organic solvents, and is stable. Its chemical properties make it widely used in organic synthesis.
Uses: (Acetyl Barterol Ester) Magnesium iodide is commonly used in the field of organic synthesis, especially alkyl, alkynyl or alkenylation reactions initiated by lithium or magnesium reagents. It can be used as an effective Grignard reagent to react with halogenated hydrocarbons or aldehyde ketals to form the corresponding alkyl, alkynyl or alkenyl magnesium reagents.
Preparation Method: (Acetobarterol Ester) Magnesium iodide is usually prepared by adding an acetic acid esterifying agent, benzidine and magnesium iodide to an acetone solution. This process can be carried out at room temperature and can be completed within a few hours.
Safety Information: (Acetobarterol Ester) Magnesium Iodide is relatively non-hazardous in general. However, as a safe handling principle for all chemical substances, appropriate laboratory precautions, including wearing protective glasses and gloves, must be used to avoid inhalation, ingestion or contact. In addition, the substance should be evaluated for safety according to the conditions and use of the specific synthesis reaction to ensure safe use in laboratory and industrial environments. In all cases, the safety data sheet and operating instructions for the substance should be reviewed.
Last Update：2024-04-10 22:29:15
