288-52-8 ((Selenazole)

快速询单

结构式：

SelenazoleMOL文件

CAS号：

288-52-8

英文名称：

Selenazole

分子式：

C₃H₃NSe

分子量：

132.022619485855

Selenazole(288-52-8)名称与标识符

名称

英文别名：

Selenazole;1,3-selenazole;1-Selena-3-azacyclopentadiene;Selenazol;SCHEMBL997340;ODIRBFFBCSTPTO-UHFFFAOYSA-;CHEMBL35736;InChI=1/C3H3NSe/c1-2-5-3-4-1/h1-3H;DTXSID70470579;288-52-8;

标识符

InChIKey：

ODIRBFFBCSTPTO-UHFFFAOYSA-N

Inchi：

1S/C3H3NSe/c1-2-5-3-4-1/h1-3H

SMILES：

[Se]1C=NC=C1

Selenazole(288-52-8)物化性质

实验特性

PSA : 12.36

计算特性

精确分子量 : 126.94909
氢键供体数量 : 0
氢键受体数量 : 1
可旋转化学键数量 : 0
同位素质量 : 132.94307g/mol
重原子数量 : 5
复杂度 : 30.1
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 : 12.9Å²

Selenazole(288-52-8)相关文献

1. A novel approach to a substituted 1,3-selenazole core as a precursor of electron rich olefins: diselenadiazafulvalene and azino-diselenadiazafulvalene
Zdenko ?asar,Alenka Majcen-Le Maréchal,Dominique Lorcy New J. Chem. 2003 27 1622
2. Route towards diselenadiazafulvalenes
Zdenko ?asar,Patricia Bénard-Rocherullé,Alenka Majcen-Le Maréchal,Dominique Lorcy Chem. Commun. 2001 1336
3. Copper-catalyzed domino synthesis of benzo[d]imidazo[5,1-b][1,3]selenazoles involving sequential intermolecular cycloaddition and intramolecular Ullmann-type C–Se bond formation
Kelu Yan,Min Liu,Jiangwei Wen,Weihua Liu,Xue Li,Xiao Liu,Xinlei Sui,Wenda Shang,Xiu Wang Org. Chem. Front. 2021 8 5139
4. Exploiting the role of stereoelectronic effects to design the antagonists of the human complement C3a receptor
Sana Jindani,Bishwajit Ganguly New J. Chem. 2021 45 9443
5. Co(iii) complexes of (1,3-selenazol-2-yl)hydrazones and their sulphur analogues
Nenad R. Filipovi?,Hana Elshaflu,Sonja Grubi?i?,Ljiljana S. Jovanovi?,Marko Rodi?,Irena Novakovi?,Aleksandar Male?evi?,Ivana S. Djordjevi?,Haidong Li,Ne?o ?oji?,Aleksandar Marinkovi?,Tamara R. Todorovi? Dalton Trans. 2017 46 2910
6. A multicomponent reaction of isocyanides, selenium powder and 3-aminooxetanes in pure water: green and efficient synthesis of 1,3-selenazolines
Huan Liu,Zi-Lin Ye,Zhong-Jian Cai,Shun-Jun Ji Green Chem. 2023 25 4239
7. New insight into the chemistry of selenoureas: synthesis and single crystal structural study of diverse derivatives
Guoxiong Hua,Junyi Du,Cameron L. Carpenter-Warren,David B. Cordes,Alexandra M. Z. Slawin,J. Derek Woollins New J. Chem. 2019 43 7035
8. Synthesis of diselenadiazafulvalenes and influence of steric strain on their anodic behavior
Zdenko C?asar,Ivan Leban,Alenka Majcen-Le Maréchal,Dominique Lorcy J. Chem. Soc. Perkin Trans. 1 2002 1568
9. Study of the effect of molecular structure and alkyl groups bound with tin(iv) on their cytotoxicity of organotin(iv) 2-phenyl-4-selenazole carboxylates
Min Hong,Yuanguang Yang,Chuan Li,Lidan Xu,Dacheng Li,Chen-zhong Li RSC Adv. 2015 5 102885
10. Unexpected ring closures leading to 2-N,N-dialkylaminoareno[1,3]tellurazoles
Johan Pierre,Zachary M. Hill,Frank R. Fronczek,Thomas Junk New J. Chem. 2022 46 22533