Description
2-Bromospiro[fluorene-9,9′-xanthene] (CAS No. 899422-06-1) is a high-purity brominated spirocyclic compound with the molecular formula C25H15BrO. This specialized organic intermediate features a unique spiro[fluorene-xanthene] core structure, offering versatile reactivity for advanced synthetic applications. The bromine substitution at the 2-position provides a reactive handle for further functionalization via cross-coupling reactions or nucleophilic substitutions. With a molecular weight of 411.29 g/mol, this compound is supplied as a crystalline solid with guaranteed ≥95% purity (HPLC). Ideal for materials science research, this building block is particularly valuable for developing organic semiconductors, photochromic materials, and fluorescent dyes. Each batch undergoes rigorous QC analysis including 1H/13C NMR, HPLC, and mass spectrometry to ensure consistency for your research needs. Store under inert atmosphere at 2-8°C protected from light.
Properties
- CAS Number: 899422-06-1
- Complexity: 539
- IUPAC Name: 2-bromospiro[fluorene-9,9′-xanthene]
- InChI: InChI=1S/C25H15BrO/c26-16-13-14-18-17-7-1-2-8-19(17)25(22(18)15-16)20-9-3-5-11-23(20)27-24-12-6-4-10-21(24)25/h1-15H
- InChI Key: MNBDZJINQUZDFP-UHFFFAOYSA-N
- Exact Mass: 410.03063
- Molecular Formula: C25H15BrO
- Molecular Weight: 411.3
- SMILES: C1=CC=C2C(=C1)C3=C(C24C5=CC=CC=C5OC6=CC=CC=C46)C=C(C=C3)Br
- Topological: 9.2
- Monoisotopic Mass: 410.03063
- Synonyms: 899422-06-1, 2-bromospiro[fluorene-9,9′-xanthene], 2-Bromospiro[9H-fluorene-9,9′-[9H]xanthene], MFCD29050113, C25H15BrO, SCHEMBL15713470, 2-Bromospiro[fluorene-9,9′-xanthene, AKOS028113687, AC-37683, DS-19403, SY078130, DB-338261, B5842, CS-0095289, F16094, 2-Bromospiro[fluorene-9,9 inverted exclamation mark -xanthene]
Application
This brominated spiro compound serves as a key intermediate in the synthesis of advanced organic materials. Researchers utilize it for developing novel fluorescent probes due to its rigid xanthene-fluorene hybrid structure. The bromine substituent enables efficient participation in palladium-catalyzed cross-coupling reactions for constructing complex π-conjugated systems. Materials scientists employ this building block in the design of organic electronic devices and photoresponsive materials.
If you are interested or have any questions, please contact us at support@atomfair.com
Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


Reviews
There are no reviews yet.