Description
3,6-Diethoxy-9H-carbazole (CAS No. 1707264-12-7) is a high-purity organic compound with the molecular formula C16H17NO2, widely utilized in advanced material science and pharmaceutical research. This carbazole derivative features ethoxy substituents at the 3- and 6-positions, enhancing its solubility and reactivity for tailored applications. With a molecular weight of 255.31 g/mol, it is supplied as a crystalline solid with ≥95% purity (HPLC), ensuring consistency for sensitive syntheses. Ideal for OLED development, photovoltaics, and as a building block for heterocyclic scaffolds, this compound is stored under inert conditions to preserve stability. Available in customizable quantities, from milligrams to kilograms, with optional analytical certificates (NMR, MS) upon request.
Properties
- CAS Number: 1707264-12-7
- Complexity: 268
- IUPAC Name: 3,6-diethoxy-9H-carbazole
- InChI: InChI=1S/C16H17NO2/c1-3-18-11-5-7-15-13(9-11)14-10-12(19-4-2)6-8-16(14)17-15/h5-10,17H,3-4H2,1-2H3
- InChI Key: NHMBEUAFNAIECC-UHFFFAOYSA-N
- Exact Mass: 255.125928785
- Molecular Formula: C16H17NO2
- Molecular Weight: 255.31
- SMILES: CCOC1=CC2=C(C=C1)NC3=C2C=C(C=C3)OCC
- Topological: 34.3
- Monoisotopic Mass: 255.125928785
- Synonyms: 3,6-Diethoxy-9H-carbazole, 1707264-12-7, SCHEMBL19583371, DB-410479
Application
3,6-Diethoxy-9H-carbazole serves as a key intermediate in the synthesis of optoelectronic materials, particularly for OLED emitters and hole-transport layers due to its conjugated structure. Researchers leverage its ethoxy groups to modify solubility for solution-processed thin films in photovoltaic devices. In medicinal chemistry, it acts as a precursor for bioactive carbazole alkaloids with potential anticancer properties. Its rigid planar framework also supports coordination chemistry in catalytic systems.
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