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| 2,4-Dibromoaniline Basic information |
| Product Name: | 2,4-Dibromoaniline | | Synonyms: | 2,4-DIBROMOANILINE;2,4-DIBROMOBENZENAMINE;2 4-DIBROMOANILINE 98% (GC);2,4-Dibromoaniline, 98+%;2,4-Dibromanilin;2,4-dibromo-benzenamin;2,4-Dibromoaniline 98%;2,4-Dibromoaniline > | | CAS: | 615-57-6 | | MF: | C6H5Br2N | | MW: | 250.92 | | EINECS: | 210-434-4 | | Product Categories: | Building Blocks;C6;Anilines, Amides & Amines;Chemical Synthesis;Nitrogen Compounds;Organic Building Blocks;Bromine Compounds;Amines;C2 to C6;Nitrogen Compounds | | Mol File: | 615-57-6.mol |
| 2,4-Dibromoaniline Chemical Properties |
| 2,4-Dibromoaniline Usage And Synthesis |
| Chemical Properties | beige powder | | Uses | 2,4-Dibromoaniline is used in preparation of glycopeptides and targeted bifunctional degraders. | | Uses | 2,4-Dibromoaniline can be used as:- A starting material to synthesize acetylenic amine by reacting with trimethylsilylacetylene, which is used as a ligand to prepare the bis-amido complex of Ti(IV).
- A substrate in the Pd-catalyzed ortho-selective cross-coupling reactions of dihaloarenes with Grignard reagents.
- A reactant to prepare dialkyl-substituted aminoaryl sulfides using a Grignard reagent.
- A starting material to synthesize substituted 2-mercapto benzimidazoles.
| | Purification Methods | Crystallise the aniline from aqueous EtOH. The picrate has m 124o. [Beilstein 12 H 655, 12 I 326, 12 II 356, 12 III 1471, 12 IV 1532.] |
| 2,4-Dibromoaniline Preparation Products And Raw materials |
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