1248439-15-7

Upstream product

• 1248336-98-2 5-((3-chlorophenyl)amino)-9-(diethylamino)benzo[a]phenoxazin-7-ium nitrate 

Downstream Products

• 1248336-98-2 5-((3-chlorophenyl)amino)-9-(diethylamino)benzo[a]phenoxazin-7-ium nitrate 
• 1248337-01-0 5-((3-chlorophenyl)amino)-9-(diethylamino)benzo[a]phenoxazin-7-ium hydrosulfate 
• 1248336-95-9 5-((3-chlorophenyl)amino)-9-(diethylamino)benzo[a]phenoxazin-7-ium chloride 
• 1248336-96-0 5-((3-chlorophenyl)amino)-9-(diethylamino)benzo[a]phenoxazin-7-ium bromide 
• 1248336-97-1 5-((3-chlorophenyl)amino)-9-(diethylamino)benzo[a]phenoxazin-7-ium iodide 
• 1248336-99-3 5-((3-chlorophenyl)amino)-9-(diethylamino)benzo[a]phenoxazin-7-ium trifluoromethanesulfonate 

Relevant academic research and scientific papers

The synthesis and third-order nonlinear optical properties of resonance Benzo[a]phenoxazinium salts

The third-order nonlinear optical properties of a series of resonance benzo[a]phenoxazinium salts in acetic acid solution were studied using the Z-scan technique employing a Nd:YAG nanosecond laser at 532 nm. The compounds displayed strong reverse absorption with third-order nonlinear optical coefficients of 0.42-1.20 × 10-11 esu and second hyperpolarizabilities of 2.75-7.29 × 10-29 esu, respectively. Quantum chemical calculations showed that the compound with more stable highest occupied molecular orbital energy also displayed highest second hyperpolarizability.