3,5-Dibromophenyl methyl ether
3,5-Dibromoanisole
CAS: 74137-36-3
Molecular Formula: C7H6Br2O
3,5-Dibromophenyl methyl ether - Names and Identifiers
| Name | 3,5-Dibromoanisole |
| Synonyms | 3,5-DibromoanisoL 3,5-DIBROMOANISOLE 3,5-Dibromoanisole 3,5-dibromophenyl ether Phloroglucinol Impurity 13 1,3-dibromo-5-methoxybenzene 1,3-Dibromo-5-methoxybenzene 3,5-Dibromophenyl methyl ether Benzene,1,3-dibroMo-5-Methoxy- benzene, 1,3-dibromo-5-methoxy- |
| CAS | 74137-36-3 |
| InChI | InChI=1/C7H6Br2O/c1-10-7-3-5(8)2-6(9)4-7/h2-4H,1H3 |
3,5-Dibromophenyl methyl ether - Physico-chemical Properties
| Molecular Formula | C7H6Br2O |
| Molar Mass | 265.93 |
| Density | 1.823 |
| Melting Point | 34-38 °C |
| Boling Point | 249.7°C |
| Flash Point | 98.1°C |
| Solubility | soluble in Methanol |
| Vapor Presure | 0.0358mmHg at 25°C |
| Appearance | White solid |
| Color | White to Gray to Brown |
| Storage Condition | Sealed in dry,Room Temperature |
| Stability | Stable. Incompatible with strong oxidizing agents. |
| Refractive Index | 1.576 |
| MDL | MFCD02258848 |
3,5-Dibromophenyl methyl ether - Risk and Safety
| Hazard Symbols | T - Toxic |
| Risk Codes | 25 - Toxic if swallowed |
| Safety Description | 45 - In case of accident or if you feel unwell, seek medical advice immediately (show the label whenever possible.) |
| UN IDs | UN 2811 6.1/PG 3 |
| WGK Germany | 3 |
| Hazard Class | 6.1 |
| Packing Group | Ⅲ |
3,5-Dibromophenyl methyl ether - Introduction
3,5-Dibromoanisole(3,5-Dibromoanisole) is an organic compound with the chemical formula C7H6Br2O. Its appearance is colorless crystals or white crystalline powder.
In terms of properties, 3,5-Dibromoanisole is poorly soluble in water, but soluble in organic solvents such as alcohols and ethers. It has the characteristics of phenol, and the chemical reaction of phenol can occur under acidic conditions.
In terms of use, 3,5-Dibromoanisole is often used as a reaction intermediate in organic synthesis. It can participate in a series of chemical reactions, such as reaction with sulfuric acid to obtain the corresponding sulfuric acid ester, reaction with ammonium chloride to obtain the corresponding chlorophenyl ether.
Regarding the preparation method, a common preparation method is to dissolve p-dibromoanisole in acetonitrile, and then add sodium iodide under alkaline conditions to react to generate 3,5-Dibromoanisole.
In terms of safety information, 3,5-Dibromoanisole is toxic and may be harmful to the environment. During use, it should be noted that it is irritating to the skin and eyes, and avoid inhaling its powder or steam. During storage and handling, good ventilation should be paid attention to and contact with oxidants and strong acids should be avoided. At the same time, storage, transportation and handling should be carried out in accordance with relevant regulations.
In terms of properties, 3,5-Dibromoanisole is poorly soluble in water, but soluble in organic solvents such as alcohols and ethers. It has the characteristics of phenol, and the chemical reaction of phenol can occur under acidic conditions.
In terms of use, 3,5-Dibromoanisole is often used as a reaction intermediate in organic synthesis. It can participate in a series of chemical reactions, such as reaction with sulfuric acid to obtain the corresponding sulfuric acid ester, reaction with ammonium chloride to obtain the corresponding chlorophenyl ether.
Regarding the preparation method, a common preparation method is to dissolve p-dibromoanisole in acetonitrile, and then add sodium iodide under alkaline conditions to react to generate 3,5-Dibromoanisole.
In terms of safety information, 3,5-Dibromoanisole is toxic and may be harmful to the environment. During use, it should be noted that it is irritating to the skin and eyes, and avoid inhaling its powder or steam. During storage and handling, good ventilation should be paid attention to and contact with oxidants and strong acids should be avoided. At the same time, storage, transportation and handling should be carried out in accordance with relevant regulations.
Last Update：2024-04-10 22:30:50
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