Products Description of 1,1,2-Trimethyl-1H-benz [e] indole CAS#41532-84-7
With the molecular-weight of 209.29 and molecular formula C15H15N, 1,1,2-trimethyl-1H-benz [e] indole belongs to the valuable alkaline-type heterocyclic raw-material. This substance appears as yellow to brown crystalline powder at ambient temperature. Its melting-point falls within 111-117 °C, and its boiling-point reaches 333.7±35.0 °C under 760-millimeter-mercury pressure. It barely dissolves in cold water and possesses good compatibility with common organic solvents.
Serving as a fundamental synthetic building-block, it is widely prepared for cyanine dyes, photochromic pigment, electroluminescent raw-materials and fine-chemical pharmaceutical intermediates.
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1,1,2-Trimethyl-1H-benz[e]indole Chemical Properties
| Melting point | 111-117 °C |
| Boiling point | 338.66°C (rough estimate) |
| density | 0.7 |
| refractive index | 1.5720 (estimate) |
| storage temp. | Inert atmosphere,Room Temperature |
| solubility | insoluble (20°C) |
| form | Crystalline Powder |
| pka | 5.77±0.40(Predicted) |
| color | Yellow to brown |
| Water Solubility | insoluble (20 ºC) |
| BRN | 153709 |
| InChI | InChI=1S/C15H15N/c1-10-15(2,3)14-12-7-5-4-6-11(12)8-9-13(14)16-10/h4-9H,1-3H3 |
| InChIKey | WJZSZXCWMATYFX-UHFFFAOYSA-N |
| SMILES | N1C2=C(C3=CC=CC=C3C=C2)C(C)(C)C=1C |
| CAS DataBase Reference | 41532-84-7(CAS DataBase Reference) |
| EPA Substance Registry System | 1H-Benz[e]indole, 1,1,2-trimethyl- (41532-84-7) |
| Hazard Codes | Xi,T |
| Risk Statements | 36/37/38-45 |
| Safety Statements | 26-36-53-45-37/39 |
| WGK Germany | 3 |
| TSCA | Yes |
| HS Code | 29339900 |
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Product Application of 1,1,2-Trimethyl-1H-benz[e]indole CAS#41532-84-7
This heterocyclic fine-chemical intermediate serves the dye-making and pharmaceutical-synthesis sectors. It acts as a fundamental building-block to prepare benz[e]indole-based cyanine dyes and multiple kinds of photochromic colourants. Thanks to its flexible chemical reactivity, the compound gets widely processed into various cyanine-dye derivatives. It also supports the manufacture of electroluminescent functional-materials and advanced drug-synthesis intermediates for laboratory-scale organic-chemistry research.
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