Anti-blue-ray system containing pyrazoline or/and cinnamic acid compounds
A compound system and anti-blue light technology, which is applied in the field of anti-blue light system, can solve the problems of no anti-blue light effect, etc., and achieve the effects of low migration, high compatibility, excellent low migration and high compatibility
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Embodiment 1
[0042] Embodiment 1 synthetic formula (I-1) compound, 1-phenyl-3-(4-butyl styryl)-5-(4-tert-butylphenyl) pyrazoline
[0043]
[0044] 16.2 g of 4-tert-butylbenzaldehyde and 3.0 g of acetone were added to the freshly prepared sodium methoxide solution and stirred at room temperature for 3 hours. After washing with water and drying, the product bis(2-(4-tert-butyl)phenylvinyl)ketone was obtained. Take 7g of bis(2-(4-tert-butyl)phenylvinyl)ketone and 2.2g of phenylhydrazine and react in acetic acid for 4 hours. After cooling, the product was purified to obtain 1-phenyl-3-(4-butylstyryl)-5-(4-tert-butylphenyl)pyrazoline with a melting point of 192-197°C. UV-VIS (ETOH.max.) 387 nm.
Embodiment 2
[0045] Example 2 Synthesis of (I-2) compound, 1-phenyl-3-(p-methoxystyryl)-5-(p-methoxyphenyl) pyrazoline
[0046]
[0047] With embodiment 1 method, but replace 4-tert-butylbenzaldehyde with p-methoxybenzaldehyde, obtain 1-phenyl-3-(p-methoxystyryl)-5-(p-methoxyphenyl ) pyrazoline (I-2) compound with a melting point of 159°C. UV-VIS (ETOH.max.) 381 nm.
Embodiment 3
[0048] Embodiment 3 synthetic formula (I-3) compound, phenyl-3-(p-methoxystyryl)-5-(p-dimethylaminophenyl) pyrazoline
[0049]
[0050] With embodiment 1 method, but replace 4-tert-butylbenzaldehyde with p-dimethylaminobenzaldehyde, obtain phenyl-3-(p-methoxystyryl)-5-(p-dimethylaminobenzaldehyde Phenyl) pyrazoline, melting point 192°C, UV-VIS (ETOH.max.) 419 nm.
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