名称和标识符别名信息物化性质相关文献专业数据库参考

Propyl,1,1,2,2,3,3,3-heptafluoro- | 3170-79-4

Propyl,1,1,2,2,3,3,3-heptafluoro-结构式图片|3170-79-4结构式图片

英文名称： Propyl,1,1,2,2,3,3,3-heptafluoro-

CAS No.： 3170-79-4

分子式： C₃HF₇

分子量： 170.02884

如需查看该化合物的详细结构式,mol文件,smile,InChi 请点击：Propyl,1,1,2,2,3,3,3-heptafluoro-结构式

PubChem CID： 137850

快速询单

Propyl,1,1,2,2,3,3,3-heptafluoro-的其他展现形式

相关化合物

六氟丙烷

HFC-236cb

CAS No.：677-56-5
1H-七氟丙烷

Propane,1,1,1,2,2,3,3-heptafluoro-

CAS No.：2252-84-8
1,1,1,2,2-五氟丙烷

Propane,1,1,1,2,2-pentafluoro-

CAS No.：1814-88-6
Propane,1,1,1,2-tetrafluoro-

CAS No.：421-48-7
1,2-Ethanediyl, 1,1,2-trifluoro-2-(trifluoromethyl)-

CAS No.：172368-65-9
ethyl,1,1,2,2,2-tetrafluoro-1-(trifluoromethyl)

CAS No.：3248-60-0

名称和标识符

InChIKey	UKACHOXRXFQJFN-UHFFFAOYSA-N
Inchi	InChI=1S/C3HF7/c4-1(5)2(6,7)3(8,9)10/h1H
SMILES	FC(C(C(F)(F)F)(F)F)F

别名信息

- 中文别名 -

- 英文别名 -

Propyl,1,1,2,2,3,3,3-heptafluoro-
1,1,1,2,2,3,3-heptafluoropropane
3170-79-4
n-C3F7
Propyl,heptafluoro

heptafluoropropyl
CLZAEVAEWSHALL-UHFFFAOYSA-N
DTXSID90185597

物化性质

实验特性

PSA	0
沸点	°Cat760mmHg
闪点	°C

计算特性

精确分子量	169.99663
氢键供体数量	0
氢键受体数量	7
可旋转化学键数量	0
同位素质量	168.988822
重原子数量	10
复杂度	111
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	0

相关文献

1. Highly efficient deep-blue phosphorescence from heptafluoropropyl-substituted iridium complexes
Jung-Bum Kim,Seung-Hoon Han,Kiyull Yang,Soon-Ki Kwon,Jang-Joo Kim,Yun-Hi Kim Chem. Commun. 2015 51 58
2. Reactions of fluoroalkyl radicals generated electrochemically. Part 2. Addition of heptafluoropropyl radicals to methyl methacrylate
Paul L. Coe,David M. Owen,Alan E. Pedler J. Chem. Soc. Perkin Trans. 1 1983 1995
3. Free radical addition to olefins. Part 8.—Addition of n-heptafluoropropyl radicals to fluoro-ethylenes
J. M. Tedder,J. C. Walton,K. D. R. Winton J. Chem. Soc. Faraday Trans. 1 1972 68 160
4. Perfluorinated 1H-indazoles and hydrotris(indazol-1-yl)borates. Supramolecular organization and a new synthetic procedure to form scorpionate ligands
Bianca K. Mu?oz,Wilfried-Solo Ojo,Kane Jacob,Nuria Romero,Laure Vendier,Emmanuelle Despagnet-Ayoub,Michel Etienne New J. Chem. 2014 38 2451
5. Oxygen transfer reactivity mediated by nickel perfluoroalkyl complexes using molecular oxygen as a terminal oxidant
Shubham Deolka,R. Govindarajan,Eugene Khaskin,Serhii Vasylevskyi,Janet Bahri,Robert R. Fayzullin,Michael C. Roy,Julia R. Khusnutdinova Chem. Sci. 2023 14 7026
6. Ionic conductivity, viscosity, and self-diffusion coefficients of novel imidazole salts for lithium-ion battery electrolytes
Anna Szcz?sna-Chrzan,Monika Vogler,Peng Yan,Gra?yna Zofia ?ukowska,Christian W?lke,Agnieszka Ostrowska,Sara Szymańska,Marek Marcinek,Martin Winter,Isidora Cekic-Laskovic,W?adys?aw Wieczorek,Helge S. Stein J. Mater. Chem. A 2023 11 13483
7. 664. Perfluoroalkyl derivatives of nitrogen. Part IV. The synthesis, properties and infrared spectra of perfluoroalkyl isocyanates and carbamates
D. A. Barr,R. N. Haszeldine J. Chem. Soc. 1956 3428
8. A study of the reaction of perfluoroalkyl Grignard reagents with phosphoryl chloride and phenylphosphonic dichloride
Adil I. Hosein,Andrew J. M. Caffyn Dalton Trans. 2012 41 13504
9. Synthetic and mechanistic aspects of the regioselective base-mediated reaction of perfluoroalkyl- and perfluoroarylsilanes with heterocyclic N-oxides
David E. Stephens,Gabriel Chavez,Martin Valdes,Monica Dovalina,Hadi D. Arman,Oleg V. Larionov Org. Biomol. Chem. 2014 12 6190
10. Interface properties and dopability of an organic semiconductor: TAPP-Br variable as molecule but inert in the condensed phase
Michael Tzschoppe,Christian Huck,Andrey Butkevich,Benjamin Günther,Constantin Ulrich,Jan Niklas Rose,Lutz H. Gade,Annemarie Pucci J. Mater. Chem. C 2020 8 9898

专业数据库参考

PubChemId	137850

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