Description
2-Bromo-9,9-bis(6-bromohexyl)-9H-fluorene (CAS No. 438201-29-7) is a highly functionalized fluorene derivative with a molecular formula of C25H31Br3. This brominated compound features a fluorene core substituted at the 2-position with a bromine atom and at the 9-position with two 6-bromohexyl chains, enhancing its reactivity and utility in organic synthesis. The presence of multiple bromine atoms makes it a versatile intermediate for cross-coupling reactions, polymerization, and material science applications. This compound is characterized by high purity and stability, making it suitable for advanced research in pharmaceuticals, OLED materials, and polymer chemistry. Proper handling under inert conditions is recommended due to its sensitivity to moisture and light.
Properties
- CAS Number: 438201-29-7
- Complexity: 424
- IUPAC Name: 2-bromo-9,9-bis(6-bromohexyl)fluorene
- InChI: InChI=1S/C25H31Br3/c26-17-9-3-1-7-15-25(16-8-2-4-10-18-27)23-12-6-5-11-21(23)22-14-13-20(28)19-24(22)25/h5-6,11-14,19H,1-4,7-10,15-18H2
- InChI Key: NXZLCKGNRSHEGW-UHFFFAOYSA-N
- Exact Mass: 569.99554
- Molecular Formula: C25H31Br3
- Molecular Weight: 571.2
- SMILES: C1=CC=C2C(=C1)C3=C(C2(CCCCCCBr)CCCCCCBr)C=C(C=C3)Br
- Monoisotopic Mass: 567.99759
- Synonyms: 2-Bromo-9,9-bis(6-bromohexyl)-9H-fluorene, 438201-29-7, 2-Bromo-9,9-bis(6-bromohexyl)fluorene, 9H-Fluorene, 2-bromo-9,9-bis(6-bromohexyl)-, SCHEMBL41469, 2-Bromo-9,9-bis-(6-bromohexyl)fluorene, DB-217097, G83511
Application
2-Bromo-9,9-bis(6-bromohexyl)-9H-fluorene is widely used as a key intermediate in the synthesis of conjugated polymers for organic electronic devices, such as OLEDs and solar cells. Its brominated structure facilitates Suzuki and Yamamoto coupling reactions, enabling the construction of complex organic frameworks. Researchers also employ this compound in the development of fluorescent probes and photoactive materials due to its rigid fluorene backbone. Additionally, it serves as a precursor for functionalized materials in nanotechnology and supramolecular chemistry.
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