890148-78-4 (2,4,6-三(3-溴苯基)-1,3,5-三嗪,2,4,6-Tris(3-bromophenyl)-1,3,5-triazine)

快速询单

结构式：

2,4,6-三(3-溴苯基)-1,3,5-三嗪MOL文件

CAS号：

890148-78-4

中文名称：

2,4,6-三(3-溴苯基)-1,3,5-三嗪

英文名称：

2,4,6-Tris(3-bromophenyl)-1,3,5-triazine

安全信息：

分子式：

C₂₁H₁₂Br₃N₃

分子量：

546.052082061768

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)名称与标识符

名称

中文别名：

2,4,6-三(3-溴苯基)-1,3,5-三嗪;2,4,6-Tris(3-bromophenyl)-1,3,5-triazine 2,4,6-三(3-溴苯基)-1,3,5-三嗪;

英文别名：

2,4,6-tris(3-bromophenyl)-1,3,5-Triazine;2,4,6-Tri(3-bromophenyl)-1,3,5-triazine;IWHHYACTSSPXDV-UHFFFAOYSA-N;tris(3-bromophenyl)-1,3,5-triazine;OL10233;AK192656;2,4,6-Tris(3-bromophenyl)-1,3,5-triazine (ACI);2,4,6-Tris(3-bromophenyl)triazine;TBrPZ;

标识符

MDL：

MFCD28964709

InChIKey：

IWHHYACTSSPXDV-UHFFFAOYSA-N

Inchi：

1S/C21H12Br3N3/c22-16-7-1-4-13(10-16)19-25-20(14-5-2-8-17(23)11-14)27-21(26-19)15-6-3-9-18(24)12-15/h1-12H

SMILES：

BrC1C=C(C2N=C(C3C=C(Br)C=CC=3)N=C(C3C=C(Br)C=CC=3)N=2)C=CC=1

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)物化性质

实验特性

沸点 : 661.4±65.0°C at 760 mmHg
熔点 : 207.0 to 211.0 deg-C

计算特性

氢键供体数量 : 0
氢键受体数量 : 3
可旋转化学键数量 : 3
重原子数量 : 27
复杂度 : 401
拓扑分子极性表面积 : 38.7

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)安全信息

符号： GHS07
危害声明：H315-H319
警示性声明：P264-P280-P302+P352+P332+P313+P362+P364-P305+P351+P338+P337+P313
提示语：警告
储存条件： Sealed in dry,Room Temperature
信号词： Warning

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)推荐厂家更多厂家(25)

公司名称	手机号/电话	联系人	QQ	询单
郑州阿尔法化工有限公司	15324716602 0371-55013243	刘经理	2853979810	询单
上海源叶生物科技有限公司	15026964105 15026964105	汤思磊	2881489226	询单
山东玖玥生物科技有限公司	15553333686	张文杰	643971	询单
JACS-郑州杰克斯化工产品有限公司	15981966935 0371-86259281	杰克斯JACS	893596907	询单
上海瀚思化工有限公司	18939883912 021-34536277	顾经理	3003949364	询单
上海创赛科技有限公司	15021221957 021-59553580	凌度	2852351983	询单
上海绩祥生物科技有限公司	13093077543	陆经理	3985448220	询单
赫澎（上海）生物科技有限公司	13122891558 186-16545970	张硕	3418426269	询单
上海腾准生物科技有限公司	19821570922 021-34053661	张经理	3003871136	询单
金锦乐（湖南）化学有限公司		金锦乐	1226360695	询单

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)合成路线

合成路线：1 步

6952-59-6

_92%

890148-78-4

反应条件：

1.1 Reagents: Trifluoromethanesulfonic acid Solvents: Dichloromethane

参考文献：

New usage for cyclotrimerization reaction. A facile synthesis of 1,3,5-triazine derivatives

Mi, Ouyang; Yu, Chun-Hui; Zhang, Ning-Yu; Song, Qing-Bao; Sun, Jing-Wei; et al, Key Engineering Materials, 2013, 531, 531-532

合成路线：1 步

6952-59-6

_73%

890148-78-4

反应条件：

1.1 Reagents: Trifluoromethanesulfonic acid Solvents: Chloroform ; 273 K; 2 h, 273 K; 3 d, 298 K
1.2 Reagents: Ammonium hydroxide Solvents: Water ; 273 K

参考文献：

Chemical signals turn on guest binding through structural reconfiguration of triangular helicates

Sorensen, Anne; Castilla, Ana M.; Ronson, Tanya K.; Pittelkow, Michael; Nitschke, Jonathan R., Angewandte Chemie, 2013, 52(43), 11273-11277

合成路线：1 步

6952-59-6

_70%

890148-78-4

反应条件：

1.1 Reagents: Trifluoromethanesulfonic acid Solvents: Chloroform ; cooled; 2 h, 0 °C; 24 h, rt
1.2 Reagents: Ammonium hydroxide Solvents: Water ; rt

参考文献：

Tuning Energy Levels of Electron-Transport Materials by Nitrogen Orientation for Electrophosphorescent Devices with an 'Ideal' Operating Voltage

Su, Shi-Jian; Sasabe, Hisahiro; Pu, Yong-Jin; Nakayama, Ken-ichi; Kido, Junji, Advanced Materials (Weinheim, 2010, 22(30), 3311-3316

合成路线：1 步

3132-99-8

_67%

890148-78-4

反应条件：

1.1 Reagents: Ammonium iodide Catalysts: Iron chloride (FeCl3) Solvents: Toluene ; 15 h, 130 °C

参考文献：

Atom-efficient synthesis of 2,4,6-trisubstituted 1,3,5-triazines via Fe-catalyzed cyclization of aldehydes with NH4I as the sole nitrogen source

Xiao, Jiang; Ren, Shuang; Liu, Qiang, RSC Advances, 2020, 10(37), 22230-22233

合成路线：1 步

6952-59-6

_67%

890148-78-4

反应条件：

1.1 Reagents: Trifluoromethanesulfonic acid Solvents: Dichloromethane ; 24 h, rt
1.2 Reagents: Sodium bicarbonate Solvents: Water ; rt

参考文献：

Electron transmission material and organic light-emitting element

, Taiwan, , ,

合成路线：1 步

6952-59-6

_67%

890148-78-4

反应条件：

1.1 Reagents: Trifluoromethanesulfonic acid Solvents: Dichloromethane ; 12 h, rt
1.2 Reagents: Sodium bicarbonate Solvents: Water ; rt

参考文献：

1,3,5-Triazine derivatives as new electron transport-type host materials for highly efficient green phosphorescent OLEDs

Chen, Hsiao-Fan; Yang, Shang-Jung; Tsai, Zhen-Han; Hung, Wen-Yi; Wang, Ting-Chih; et al, Journal of Materials Chemistry, 2009, 19(43), 8112-8118

合成路线：1 步

6952-59-6

_65%

890148-78-4

反应条件：

1.1 Reagents: Trifluoromethanesulfonic acid Solvents: Chloroform ; 0 °C; 0 °C → rt; 24 h, rt
1.2 Solvents: Water ; 2 h, rt

参考文献：

Triazine-phosphine oxide electron transporter for ultralow-voltage-driven sky blue PHOLEDs

Jia, Jilin; Zhu, Liping; Wei, Ying; Wu, Zhongbin; Xu, Hui; et al, Journal of Materials Chemistry C: Materials for Optical and Electronic Devices, 2015, 3(19), 4890-4902

合成路线：1 步

6952-59-6

_59%

890148-78-4

反应条件：

1.1 Reagents: Trifluoromethanesulfonic acid Solvents: Dichloromethane ; overnight, rt

参考文献：

Engineering the Interconnecting Position of Star-Shaped Donor-π-Acceptor Molecules Based on Triazine, Spirofluorene, and Triphenylamine Moieties for Color Tuning from Deep Blue to Green

Wang, Yafei; Liu, Wanhui; Deng, Jiyong; Xie, Guohua; Liao, Yuanwei; et al, Chemistry - An Asian Journal, 2016, 11(18), 2555-2563

合成路线：1 步

6952-59-6

890148-78-4

反应条件：

1.1 Reagents: Trifluoromethanesulfonic acid Solvents: Dichloromethane

参考文献：

Rational utilization of intramolecular and intermolecular hydrogen bonds to achieve desirable electron transporting materials with high mobility and high triplet energy

Yin, Xiaojun; Chen, Dongcheng; Peng, Qiming; Xiang, Yepeng; Xie, Guohua; et al, Journal of Materials Chemistry C: Materials for Optical and Electronic Devices, 2016, 4(7), 1482-1489

合成路线：1 步

6952-59-6

890148-78-4

反应条件：

1.1 Reagents: Trifluoromethanesulfonic acid

参考文献：

Thermally activated delayed fluorescence of N-phenylcarbazole and triphenylamine functionalized tris(aryl)triazines

Huang, Bin; Yin, Zhihui; Ban, Xinxin; Jiang, Wei; Dai, Yu; et al, Dyes and Pigments, 2015, 117, 141-148

合成路线：1 步

6952-59-6

890148-78-4

反应条件：

1.1 Reagents: Trifluoromethanesulfonic acid Solvents: Chloroform

参考文献：

A novel, bipolar host based on triazine for efficient solution-processed single-layer green phosphorescent organic light-emitting diodes

Huang, Bin; Jiang, Wei; Tang, Jinan; Ban, Xinxin; Zhu, Ruigang; et al, Dyes and Pigments, 2014, 101, 9-14

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)相关文献

1. Functionalized 1,3,5-triazine derivatives as components for photo- and electroluminescent materials
Emiliya V. Nosova,Galina N. Lipunova,Grigory V. Zyryanov,Valery N. Charushin,Oleg N. Chupakhin Org. Chem. Front. 2022 9 6646
2. Novel triazine derivatives with deep LUMO energy levels as the electron-accepting components of exciplexes
Jing Guo,Cai-Jun Zheng,Ke Ke,Ming Zhang,Hao-Yu Yang,Jue-Wen Zhao,Ze-Yu He,Hui Lin,Si-Lu Tao,Xiao-Hong Zhang J. Mater. Chem. C 2021 9 939
3. Rational utilization of intramolecular and intermolecular hydrogen bonds to achieve desirable electron transporting materials with high mobility and high triplet energy
Xiaojun Yin,Dongcheng Chen,Qiming Peng,Yepeng Xiang,Guohua Xie,Zece Zhu,Cheng Zhong,Feng Li,Shijian Su,Chuluo Yang J. Mater. Chem. C 2016 4 1482
4. Highly efficient exciplex emission in solid-state light-emitting electrochemical cells based on mixed ionic hole-transport triarylamine and ionic electron-transport 1,3,5-triazine derivatives
Hsiao-Fan Chen,Chih-Teng Liao,Hai-Ching Su,Yun-Shiuan Yeh,Ken-Tsung Wong J. Mater. Chem. C 2013 1 4647
5. Exciplex polymer with strong AIE for constructing fully-solution-processed organic light-emitting diodes with 100-fold efficiency improvement compared to physically blended exciplex
Xinxin Ban,Suyu Qiu,Qingpeng Cao,Kaizhi Zhang,Tao Zhou,Hui Xu,Ming Pei,Fengjie Ge,Zhiwei Tong,Wei Jiang Polym. Chem. 2022 13 6500

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)参考资料

Reaxys RN：

15530384

PubChem CID：

253661290

80563-82-2(二甲氧基苯磺酰氯) 80563-87-7(Methyl 2-chloro-6-nitrobenzoate) 80538-72-3(4-乙酰-烟酰胺) 80543-51-7(O-FORMYLMANDELOYL CHLORIDE) 80584-92-5(三嗪聚羧酸三乙醇胺盐 Irgacor L184) 807295-35-8(2,4-IMIDAZOLIDINEDIONE, 5-(4-PIPERIDINYL)-) 807319-94-4((2S)-1-Isopropyl-2-methylpiperazine) 80812-32-4(3-(p-Tolylsulfonylamino)-5-fluorouracil)

问答

960化工网为您提供2,4,6-三(3-溴苯基)-1,3,5-三嗪专业化合物百科信息，包括中文名，英文名，分子式，分子量，以及该化合物的CasNo.890148-78-4,相关理化性质;并提供了优质生产厂家信息包括厂家名称和联系方式等。 WAP版:890148-78-4 国际站:890148-78-4

890148-78-4 (2,4,6-三(3-溴苯基)-1,3,5-三嗪,2,4,6-Tris(3-bromophenyl)-1,3,5-triazine)

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)名称与标识符

名称

标识符

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)物化性质

实验特性

计算特性

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)安全信息

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)推荐厂家 更多厂家(25)

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)合成路线

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)相关文献

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)参考资料

目录

2,4,6-三(3-溴苯基)-1,3,5-三嗪(890148-78-4)推荐厂家更多厂家(25)