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| 4-Bromobenzaldehyde Basic information |
| 4-Bromobenzaldehyde Chemical Properties |
Hazard Codes | Xn,Xi | Risk Statements | 22-36/37/38-43 | Safety Statements | 26-36/37-36/37/39-22 | RIDADR | 2811 | WGK Germany | 2 | RTECS | CU4810000 | Hazard Note | Irritant/Harmful/Air Sensitive | TSCA | Yes | HazardClass | 6.1(b) | PackingGroup | III | HS Code | 29130000 |
| 4-Bromobenzaldehyde Usage And Synthesis |
Chemical Properties | white crystalline solid | Uses | Employed in palladium-catalyzed mono- and bis-arylation of 3,4-(ethylenedioxy)thiophenes. Also used in a cross-coupling study with potassium vinyltrifluoroborate. | Uses | 4-Bromobenzaldehyde is widely utilized as an intermediate for the preparation of agrochemicals, pharmaceuticals and other organic compounds. It is used as a precursor and reacts with sulfamethoxazole to prepare Schiff?s base, 4-[(4-Bromo-benzylidene)-amino]-N-(5-methyl-isoxazol-3-yl)-benzene sulfonamide, which can be used for the photo stability of polyvinyl chloride (PVC). It plays an important role in palladium-catalyzed mono- and bis-arylation of 3,4-(ethylenedioxy)thiophenes. It is employed in a cross-coupling study with potassium vinyltrifluoroborate. | Synthesis Reference(s) | Journal of the American Chemical Society, 81, p. 4113, 1959 DOI: 10.1021/ja01524a080 Tetrahedron Letters, 21, p. 813, 1980 DOI: 10.1016/S0040-4039(00)71512-7 |
| 4-Bromobenzaldehyde Preparation Products And Raw materials |
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