7304-91-8 (((phenylseleninyl)benzene)

快速询单

结构式：

(phenylseleninyl)benzeneMOL文件

CAS号：

7304-91-8

英文名称：

(phenylseleninyl)benzene

分子式：

C₁₂H₁₀OSe

分子量：

249.167202472687

(phenylseleninyl)benzene(7304-91-8)名称与标识符

名称

英文别名：

(phenylseleninyl)benzene;Diphenyl selenoxide;phenylseleninylbenzene;Diphenylselenium oxide;Phenyl selenoxide;SCHEMBL158572;Benzene,1'-seleninylbis-;Benzene, 1,1'-seleninylbis-;diphenylselenoxide;7304-91-8;(Phenylseleninyl)benzene #;DTXSID70308348;AKOS004906811;NSC203208;NSC-203208;1,1?-Seleninylbis[benzene]; Phenyl Selenoxide; Diphenyl Selenoxide; Diphenylselenide Oxide; Diphenylselenium Oxide; NSC 203208;

标识符

InChIKey：

OOZCGWBPTPQVFX-UHFFFAOYSA-N

Inchi：

1S/C12H10OSe/c13-14(11-7-3-1-4-8-11)12-9-5-2-6-10-12/h1-10H

SMILES：

[Se](C1C=CC=CC=1)(C1C=CC=CC=1)=O

(phenylseleninyl)benzene(7304-91-8)物化性质

实验特性

PSA : 17.07

计算特性

精确分子量 : 243.9957
氢键供体数量 : 0
氢键受体数量 : 1
可旋转化学键数量 : 2
同位素质量 : 249.98969g/mol
重原子数量 : 14
复杂度 : 171
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 : 17.1Å²

(phenylseleninyl)benzene(7304-91-8)相关文献

1. Hydrogen bonding in some adducts of oxygen bases with acids. Part 7.—Thermodynamic study by infra-red spectroscopy of the association of chloroacetic acids with some oxygen bases
D. Had?i,J. Rajnvajn J. Chem. Soc. Faraday Trans. 1 1973 69 151
2. Evidence of an equilibrium between selenides and osmium(viii) reagents and selenoxides and osmium(vi) reagents
Alain Krief,Alexandra Destree,Virginie Durisotti,Nicolas Moreau,Caroline Smal,Catherine Colaux-Castillo Chem. Commun. 2002 558
3. Evidence of an equilibrium between selenides and osmium(viii) reagents and selenoxides and osmium(vi) reagents
Alain Krief,Alexandra Destree,Virginie Durisotti,Nicolas Moreau,Caroline Smal,Catherine Colaux-Castillo Chem. Commun. 2002 558
4. Hydrogen bonding in some adducts of oxygen bases with acids. Part II. Infrared spectra of liquid adducts of carboxylic acids with sulphoxides, phosphine oxides, and other bases
D. Had?i,N. Kobilarov J. Chem. Soc. A 1966 439
5. An infrared study on benzeneseleninic acids and salts: assignments and substituent effects
D. De Filippo,F. Momicchioli,A. Rastelli,C. Preti,G. Verani J. Chem. Soc. B 1971 1065
6. Recent advances in synthesis of stilbene derivatives via cross-coupling reaction
Fatemeh Doraghi,Faeze Yousefnejad,Soghra Farzipour,Seyedeh Pegah Aledavoud,Bagher Larijani,Mohammad Mahdavi Org. Biomol. Chem. 2023 21 1846
7. Synthesis, structure and reactivity of [o-(2,6-diisopropylphenyliminomethinyl)phenyl]selenenyl selenocyanate (RSeSeCN) and related derivatives
Prakul Rakesh,Harkesh B. Singh,Jerry P. Jasinski,James A. Golen Dalton Trans. 2014 43 9431
8. Novel acylation of a vinyl group by the reaction of an aldehyde and a vinylselenonium ylide
Shin-ichi Watanabe,Tomokazu Kusumoto,Chikayo Yoshida,Tadashi Kataoka aldehyde and a vinylselenonium ylide. Shin-ichi Watanabe Tomokazu Kusumoto Chikayo Yoshida Tadashi Kataoka Chem. Commun. 2001 839
9. Preparation of selenoxides from the catalytic autoxidation of organoselenides with nitrogen oxides
Eric Bosch,Jay K. Kochi J. Chem. Soc. Perkin Trans. 1 1996 2731
10. CCXCIX.—The quadrivalency of selenium. Part III. The instability of the compounds of quadrivalent selenium derived from phenyl methyl and phenyl ethyl selenides and phenyl- and p-tolyl-seleno-glycollie acids
Owen Kempster Edwards,Wilson Robinson Gaythwaite,Joseph Kenyon,Henry Phillips J. Chem. Soc. 1928 2293