Description
1-(9,9-Dimethyl-9H-fluoren-2-yl)isoquinoline (CAS No. 435277-99-9) is a high-purity organic compound with the molecular formula C24H19N. This specialized chemical features a unique structural combination of a dimethylfluorene moiety and an isoquinoline group, making it valuable for advanced research applications. With a molecular weight of 321.42 g/mol, this compound is ideal for use in materials science, organic synthesis, and photophysical studies. Its rigid, conjugated structure lends itself to applications in optoelectronic materials, including OLEDs and organic semiconductors. Available in research quantities, this product is rigorously tested for purity and consistency, ensuring reliable performance in your laboratory.
Properties
- CAS Number: 435277-99-9
- Complexity: 482
- IUPAC Name: 1-(9,9-dimethylfluoren-2-yl)isoquinoline
- InChI: InChI=1S/C24H19N/c1-24(2)21-10-6-5-9-19(21)20-12-11-17(15-22(20)24)23-18-8-4-3-7-16(18)13-14-25-23/h3-15H,1-2H3
- InChI Key: UCAPEQBJBMYCNV-UHFFFAOYSA-N
- Exact Mass: 321.151749610
- Molecular Formula: C24H19N
- Molecular Weight: 321.4
- SMILES: CC1(C2=CC=CC=C2C3=C1C=C(C=C3)C4=NC=CC5=CC=CC=C54)C
- Topological: 12.9
- Monoisotopic Mass: 321.151749610
- Synonyms: 1-(9,9-Dimethyl-9H-fluoren-2-yl)isoquinoline, 435277-99-9, DTXSID90591336, DTXCID30542100, 1-(9,9-DIMETHYLFLUOREN-2-YL)ISOQUINOLINE, 1-(9,9-Dimethyl-9H-fluoren-2-yl)-isoquinoline, (9,9-dimethylfluoren-2-yl)isoquinoline, 1-(9,9-Dimethylfluuoren-2-yl)isoquinoline, SCHEMBL2174684, SBB059716, AKOS016014081, 1-(9,9-dimethylfluorene-2-yl)isoquinoline, 1-(9,9-dimethylfluorene-2-yl) isoquinoline, CS-0435203, ST51044621, 1-(9,9-dimethyl-9h-fluoren-2-yl) isoquinoline
Application
1-(9,9-Dimethyl-9H-fluoren-2-yl)isoquinoline is primarily used in the development of organic electronic materials due to its conjugated aromatic system. Researchers employ this compound in the synthesis of novel optoelectronic materials, such as light-emitting diodes (OLEDs) and photovoltaic devices. Its structural properties also make it a candidate for studying charge transport mechanisms in organic semiconductors. Additionally, it serves as a building block for more complex heterocyclic systems in medicinal chemistry research.
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