16189-35-8 (CYCLOPENTYLIDENECYCLOPENTANE,Cyclopentylidenecyclopentane)

快速询单

结构式：

CYCLOPENTYLIDENECYCLOPENTANEMOL文件

CAS号：

16189-35-8

中文名称：

CYCLOPENTYLIDENECYCLOPENTANE

英文名称：

Cyclopentylidenecyclopentane

分子式：

C₁₀H₁₆

分子量：

136.234043121338

CYCLOPENTYLIDENECYCLOPENTANE(16189-35-8)名称与标识符

名称

中文别名：

CYCLOPENTYLIDENECYCLOPENTANE;

英文别名：

Cyclopentylidenecyclopentane;1,1'-bi(cyclopentylidene);AKOS006271858;δ(1,1')-bicyclopentylidene;Cyclopentane, cyclopentylidene-;CHEBI:36822;CTK0A9662;AC1LC70Z;bicyclopentylidene;Bicyclopentyliden;Bicyclopentyliden;Cyclopentane,cyclopentylidene;bicyclopentylidene;;16189-35-8;DTXSID50338441;Delta(1,1')-bicyclopentylidene;AFQHVWWURXWNGD-UHFFFAOYSA-N;Q27116975;

标识符

InChIKey：

AFQHVWWURXWNGD-UHFFFAOYSA-N

Inchi：

1S/C10H16/c1-2-6-9(5-1)10-7-3-4-8-10/h1-8H2

SMILES：

C1(/CCCC/1)=C1/CCCC/1

CYCLOPENTYLIDENECYCLOPENTANE(16189-35-8)物化性质

实验特性

LogP : 3.43100
PSA : 0.00000

计算特性

精确分子量 : 136.12500
氢键供体数量 : 0
氢键受体数量 : 0
可旋转化学键数量 : 0
同位素质量 : 136.125200510g/mol
重原子数量 : 10
复杂度 : 119
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
疏水参数计算参考值（XlogP） : 2.9
拓扑分子极性表面积 : 0Å²

CYCLOPENTYLIDENECYCLOPENTANE(16189-35-8)相关文献

1. Ruthenium-catalysed cyclisation reactions of 1,11-dien-6-ynes leading to biindenes
Takanori Matsuda,Naoto Yonekubo Org. Biomol. Chem. 2020 18 1760
2. The properties of bicyclic and multicyclic hydrocarbons as bio-derived compression ignition fuels that can be prepared via efficient and scalable routes from biomass
Lelia Cosimbescu,Kristen B. Campbell,Senthil Subramanian,Marie S. Swita,Naijia Hao,Cameron M. Moore,Karthikeyan K. Ramasamy,Andrew D. Sutton,Charles S. McEnally,Lisa D. Pfefferle,Junqing Zhu Sustainable Energy Fuels 2021 5 3143
3. Research progress of catalysts for aldol condensation of biomass based compounds
Xing Zhang,YanQing Li,Chi Qian,Ling An,Wei Wang,XiuFeng Li,XianZhao Shao,Zhizhou Li RSC Adv. 2023 13 9466
4. Butterflyene: an entry into an aesthetically pleasing carbocycle via a Diels–Alder reaction on a tetrasubstituted olefin
Gaurang J. Bhatt,Pradeep T. Deota,Narayan N. Som,Darshil Shah Org. Biomol. Chem. 2023 21 7917
5. Catalysis of ene reactions by lithium perchlorate
Alwyn G. Davies,Wojciech J. Kinart J. Chem. Soc. Perkin Trans. 2 1993 2281
6. Stereoselectivity in the Ene reaction of syn- and anti-1-(4-tert-butylcyclohexylidene)-4-tert-butylcyclohexane with singlet oxygen, nitrosyl hydride, nitrosoformaldehyde, 4-phenyl-1,2,4-triazol-3,5-dione, diethyl azodicarboxylate and methyl propiolate
Hai-Shan Dang,Alwyn G. Davies J. Chem. Soc. Perkin Trans. 2 1991 721
7. A new one-flask Ramberg–B?cklund reaction
Tze-Lock Chan,Sun Fong,Yu Li,Tim-On Man,Chi-Duen Poon J. Chem. Soc. Chem. Commun. 1994 1771
8. Waste HD-PE plastic, deformation into liquid hydrocarbon fuel using pyrolysis-catalytic cracking with a CuCO3 catalyst
Man Vir Singh,Sudesh Kumar,Moinuddin Sarker Sustainable Energy Fuels 2018 2 1057
9. Photochemically-induced 1,3-fluorine shifts. The synthesis of novel fluorinated spiro compounds
Martin R. Bryce,Richard D. Chambers,Graham Taylor J. Chem. Soc. Chem. Commun. 1983 1457
10. Novel derivatives of perfluorocyclobutene
Richard D. Chambers,Graham Taylor,Richard L. Powell J. Chem. Soc. Chem. Commun. 1978 433

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