4-Bromobenzaldehyde oxime (TCI B6593, CAS 34158-73-1) combines a reactive aldoxime group with a bromine-substituted aromatic ring. The oxime serves as a precursor to nitrile oxides for 1,3-dipolar cycloadditions that build isoxazole and isoxazoline scaffolds. The aryl bromide remains available afterwards for cross-coupling reactions such as Suzuki or Sonogashira, enabling controlled two-stage elaboration. The 100 mg pack size suits small-scale synthetic research, reaction screening, and reference preparation.
—
| Brand | — |
|---|---|
| CAS number | — |
| Molecular formula | — |
| Purity | — |
| Category | — |
| Pack sizes | — |
| Physical form | — |
| Storage | — |
—
- Ward et al. (2001). Crystal structure of syn-4-bromobenzaldehyde oxime, CyHeBrNO. Zeitschrift für Kristallographie - New Crystal Structures doi:10.1524/ncrs.2001.216.14.597
- Ward et al. (2001). Crystal structure of anti'-4-bromobenzaldehyde oxime, C7H6BrNO. Zeitschrift für Kristallographie - New Crystal Structures doi:10.1524/ncrs.2001.216.14.595
- Zonouzi et al. (2011). (E)-2-Bromobenzaldehyde oxime. Acta Crystallographica Section E Structure Reports Online doi:10.1107/s1600536811032211
References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.
