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| | 1-Bromo-2-methoxyethane Basic information |
| Product Name: | 1-Bromo-2-methoxyethane | | Synonyms: | 2-Bromoethyl methyl ether, 95%, stab. with sodium carbonate;Methyl 2-bromoethyl ether;2-Bromoethyl methyl ether,95%;2-Bromoethyl methyl ether 98%;1-Bromo-2-methoxyethane, 1-Bromo-3-oxabutane;2-BroMoethyl Methyl Ether , 95.0%(GC);2 - broMine ethyl Methyl ether;1-Bromo-2-methoxyethane (stabilised) for synthesis | | CAS: | 6482-24-2 | | MF: | C3H7BrO | | MW: | 138.99 | | EINECS: | 229-339-4 | | Product Categories: | Erlotinib | | Mol File: | 6482-24-2.mol |  |
| | 1-Bromo-2-methoxyethane Chemical Properties |
| Hazard Codes | Xi,F,Xn | | Risk Statements | 10-36/37/38-22 | | Safety Statements | 16-26-37/39 | | RIDADR | UN 3271 3/PG 3 | | WGK Germany | 3 | | Hazard Note | Irritant/Flammable | | TSCA | T | | HazardClass | 3 | | PackingGroup | III | | HS Code | 29091990 |
| | 1-Bromo-2-methoxyethane Usage And Synthesis |
| Chemical Properties | clear colorless to yellow liquid | | Uses | 2-Bromoethyl methyl ether has been used as starting reagent in the synthesis of 1-bromo-4-(2-methoxyethoxy)benzene and 1-bromo-4-[(2-methoxyethoxy)methyl]benzene. | | Uses | 1-Bromo-2-methoxyethane has been used as starting reagent in the synthesis of 1-bromo-4-(2-methoxyethoxy)benzene and 1-bromo-4-[(2-methoxyethoxy)methyl]benzene.
| | General Description | Kinetics of potassium iodide exchange reaction with 2-bromoethyl methyl ether in acetone at 15 and 25°C has been investigated. |
| | 1-Bromo-2-methoxyethane Preparation Products And Raw materials |
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