- 英文名称2-(3-Bromo-5-Chlorophenyl)-4,6-Diphenyl-1,3,5-Triazine
- 中文名称2-(3-溴-5-氯苯基)-4,6-二苯基-1,3,5三嗪
- IUPAC名称2-(3-bromo-5-chlorophenyl)-4,6-diphenyl-1,3,5-triazine
- 其它别名2-(3-Bromo-5-Chlorophenyl)-4,6-Diphenyl-1,3,5-Triazine; 1,3,5-Triazine, 2-(3-Bromo-5-Chlorophenyl)-4,6-Diphenyl-
- CAS编号1073062-42-6
- MFCD编号:MFCD28559269
- EINECS号:188-367-4
- 分子式:C21H13BrClN3
- 分子量:422.71
- 产品CID: 111688
- 产品分类有机原料 → 苯类化合物 → 苯取代衍生物
欧盟法规
C&L通报上下游产品
2-氯-4,6-二苯基-1,3,5-三嗪 2-Chloro-4,6-Diphenyl-1,3,5-Triazine 3842-55-5合成工艺路线路线简述
- 合成目标产物 2-(3-Bromo-5-Chlorophenyl)-4,6-Diphenyl-1,3,5-Triazine 主要起始原料 3-Bromo-5-Chloro-Benzaldehyde And Benzamidine Hydrochloride
- (文献来源)合成步骤主要原料 3-Bromo-5-Chloro-Benzaldehyde 和 Benzamidine Hydrochloride
1,3-二溴-5-氯苯置于lithium Chloro-Isopropyl-Magnesium Chloride体系中,用 四氢呋喃,甲苯 用作溶剂,化学反应 28.5H,反应生成2-(3-溴-5-氯苯基)-4,6-二苯基-1,3,5三嗪
参考文献:トリアリールトリアジン化合物の製造方法
标题:トリアリールトリアジン化合物の製造方法
摘要:这是一个合成有机电致发光器件中使用的电荷传输材料的中间体,对于三芳基三嗪化合物的简便且廉价的制备方法的问题.解决方法是通过将具有两种不同芳香基的2-苯基-4,6-二氯三嗪化合物与特定芳基格氏试剂反应来制备三芳基三嗪化合物.代表性化合物为:2-(3-溴-5-氯苯基)-4,6-二苯基-1,3,5-三嗪.[选择图]无
专利信息
专利号:US-2025042877-A1
优先权日:2021-11-30
标题:Organic compound, organic device, light-emitting apparatus, and electronic appliance
发明人:HAYASHI YUKI; KAWAKAMI SACHIKO; HASHIMOTO NAOAKI
权利人:SEMICONDUCTOR ENERGY LAB
摘要:A novel compound, a synthesis method thereof, and an organic device including the novel compound are provided. A compound represented by General Formula (G1) is provided. In General Formula (G1), each of R1, R2, and R5 to R7 independently represents any of hydrogen (including deuterium), an alkyl group having 1 to 10 carbon atoms, a substituted or unsubstituted aryl group having 1 to 60 carbon atoms, and a substituted or unsubstituted heteroaryl group having 1 to 60 carbon atoms. R3 represents a condensed ring composed of 4 to 10 rings containing nitrogen as an element forming the ring, and R4 represents any of a substituted or unsubstituted condensed ring having 1 to 60 carbon atoms, a substituted or unsubstituted aryl group with a molecular weight of 78 or more, and a substituted or unsubstituted heteroaryl group with a molecular weight of 80 or more. At least one of A1 to A3 represents nitrogen, and each of the others represents substituted carbon. Each of substituents of A1 to A3 independently represents any of hydrogen (including deuterium), an alkyl group having 1 to 10 carbon atoms, a substituted or unsubstituted aryl group having 1 to 60 carbon atoms, and a substituted or unsubstituted heteroaryl group having 1 to 60 carbon atoms.