22706-23-6 ((2lambda4,1,3-benzoselenadiazole)

快速询单

结构式：

2lambda4,1,3-benzoselenadiazoleMOL文件

CAS号：

22706-23-6

英文名称：

2lambda4,1,3-benzoselenadiazole

分子式：

C₆H₄N₂Se

分子量：

183.069359779358

2lambda4,1,3-benzoselenadiazole(22706-23-6)名称与标识符

名称

英文别名：

benzoselenadiazole, 2,1,3-;2lambda4,1,3-benzoselenadiazole;UNII-44Z4759EKU;T70699;EINECS 205-986-8;Piazselenol;2;A2-2,1,3-Benzoselenadiazole;AG-690/11353667;273-15-4;22706-23-6;MFCD00022886;Benzo-1,2,5-selenadiazole;Piaselenole;Piazselenole;B4313;NS00079424;BBL012553;Benzo-2,1,3-selenadiazole;EN300-17451;NSC-408467;2,3-Benzoselenadiazole;SCHEMBL766609;44Z4759EKU;NSC 408467;DTXSID60181743;InChI=1/C6H4N2Se/c1-2-4-6-5(3-1)7-9-8-6/h1-4;NSC408467;J-016729;Phenylpiazselenole;Z56941035;3,4-Benzo-1,2,5-selenadiazole;3,2,5-selenadiazole;2-Selena-1,3-diaza-2H-isoindene;AKOS000279187;2,1,3-Benzoselenadiazole;AI3-52289;2,1,3-Benzoselenadiazole-2-SeIV;AKOS001040672;CS-0356772;Benzo-2,3-selenadiazole;E4;STK743029;benzo[c][1,2,5]selenadiazole;

标识符

InChIKey：

AYTPIVIDHMVGSX-UHFFFAOYSA-N

Inchi：

1S/C6H4N2Se/c1-2-4-6-5(3-1)7-9-8-6/h1-4H

SMILES：

[Se]1N=C2C=CC=CC2=N1

2lambda4,1,3-benzoselenadiazole(22706-23-6)物化性质

实验特性

PSA : 24.72

计算特性

精确分子量 : 177.96002
氢键供体数量 : 0
氢键受体数量 : 2
可旋转化学键数量 : 0
同位素质量 : 183.95397g/mol
重原子数量 : 9
复杂度 : 95.2
同位素原子数量 : 0
确定原子立构中心数量 : 0
不确定原子立构中心数量 : 0
确定化学键立构中心数量 : 0
不确定化学键立构中心数量 : 0
共价键单元数量 : 1
拓扑分子极性表面积 : 25.8Å²

2lambda4,1,3-benzoselenadiazole(22706-23-6)相关文献

1. Enhancement of cell uptake and antitumor activity of selenadiazole derivatives through interaction and delivery by serum albumin
Shulin Deng,Delong Zeng,Yi Luo,Jianfu Zhao,Xiaoling Li,Zhennan Zhao,Tianfeng Chen RSC Adv. 2017 7 16721
2. Selenadiazole derivatives antagonize glucocorticoid-induced osteoblasts cells apoptosis by blocking ROS-mediated signaling, a new anti-osteoporosis strategy
Yanxin Du,Hong Li,Bolai Chen,Haoqiang Lai,Xiaoling Li,Tianfeng Chen RSC Adv. 2017 7 29656
3. Molecular weight and end capping effects on the optoelectronic properties of structurally related ‘heavy atom’ donor–acceptor polymers
Gregory L. Gibson,Dong Gao,Ashlee A. Jahnke,Jing Sun,Andrew J. Tilley,Dwight S. Seferos J. Mater. Chem. A 2014 2 14468
4. On the inverse correlation between the hydrogen bond strength and chalcogen bond strength in the cyclic supramolecular heterosynthon [–Se–N]?[HOOC–]
Honghong Lan,Shaobin Miao,Yu Zhang,Weizhou Wang CrystEngComm 2023 25 2159
5. Effective modulation of the photoluminescence properties of 2,1,3-benzothiadiazoles and 2,1,3-benzoselenadiazoles by Pd-catalyzed C–H bond arylations
Imane Idris,Thibault Tannoux,Fazia Derridj,Vincent Dorcet,Julien Boixel,Veronique Guerchais,Jean-Fran?ois Soulé,Henri Doucet J. Mater. Chem. C 2018 6 1731
6. The effect of single atom substitution (O, S or Se) on photocatalytic hydrogen evolution for triazine-based conjugated porous polymers
Jie Yu,Shufang Chang,Xiaoxiang Xu,Xiaoming He,Chi Zhang J. Mater. Chem. C 2020 8 8887
7. Red electroluminescent polyfluorenes containing highly efficient 2,1,3-benzoselenadiazole- and 2,1,3-naphthothiadiazole-based red dopants in the side chain
Lei Chen,Hui Tong,Zhiyuan Xie,Lixiang Wang,Xiabin Jing,Fosong Wang J. Mater. Chem. 2011 21 15773
8. Color tuning of Novel 2,1,3-Naphthothiadiazole and 2,1,3-Benzoselenadiazole based D-A-D′ Type dopants to realize highly efficient saturated red emission in non-polar solvents
Lei Chen,Lixiang Wang,Xiabin Jing,Fosong Wang J. Mater. Chem. 2011 21 10265
9. Effects of the acceptor pattern and substitution position on the properties of N-phenyl-carbazolyl based donor–acceptor–donor molecules
Xuejing Song,Min Wang,Lingqian Kong,Jinsheng Zhao RSC Adv. 2017 7 18189
10. 2-(2,3,4,5,6-Pentafluorophenyl)-1H-benzo[d]imidazole, a fluorine-rich building block for the preparation of conjugated polymer donors for organic solar cell applications
Marios Neophytou,Heraklidia A. Ioannidou,Theodosia A. Ioannou,Christos L. Chochos,Solon P. Economopoulos,Panayiotis A. Koutentis,Grigorios Itskos,Stelios A. Choulis Polym. Chem. 2012 3 2236

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