262145
Perfluorohexyl iodide
99%
동의어(들):
Tridecafluoro-1-iodohexane, 1-Iodoperfluorohexane, 1-Iodotridecafluorohexane, Tridecafluorohexyl iodide
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모든 사진(1)
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5 G
₩88,204
25 G
₩134,894
About This Item
Linear Formula:
CF3(CF2)5I
CAS Number:
Molecular Weight:
445.95
Beilstein:
1802118
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
99%
양식
liquid
refractive index
n20/D 1.329 (lit.)
bp
117 °C (lit.)
density
2.063 g/mL at 25 °C (lit.)
작용기
fluoro
iodo
SMILES string
FC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(F)I
InChI
1S/C6F13I/c7-1(8,3(11,12)5(15,16)17)2(9,10)4(13,14)6(18,19)20
InChI key
BULLJMKUVKYZDJ-UHFFFAOYSA-N
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일반 설명
Perfluorohexyl iodide forms 1:1 complexes with a variety of hydrogen-bond acceptors[1]. It has been grafted onto the isocitronellene/propene copolymer by radical reaction yielding a poly(α-olefin) with fluorinated side chains[2]. The radical addition of perfluorohexyl iodide to vinyl acetate, using azo-bis( isobutyronitrile) (AIBN) as an initiator, has been investigated[3].
Storage Class Code
10 - Combustible liquids
WGK
WGK 1
Flash Point (°F)
239.0 °F - closed cup
Flash Point (°C)
115 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
이미 열람한 고객
Effect of reaction conditions on the radical addition of perfluorohexyl iodide to vinyl acetate.
Napoli M, et al.
Journal of Fluorine Chemistry, 57(1), 219-227 (1992)
Rafel Cabot et al.
Chemical communications (Cambridge, England), (15)(15), 2005-2007 (2009-04-01)
Quantitative studies of the 1 : 1 complexes formed between perfluorohexyl iodide and a variety of hydrogen-bond acceptors have been used to probe the relationship between halogen bonding, hydrogen bonding, desolvation and the electrostatics of non-covalent interactions.
Alexander A Marchione et al.
Journal of magnetic resonance (San Diego, Calif. : 1997), 286, 143-147 (2017-12-16)
A train of BURBOP universal rotation pulses has been used to generate a spin lock sufficient to observe TOCSY correlations over a 46 kHz
Zirconocene-MAO-catalyzed homo-and copolymerizations of linear asymmetrically substituted dienes with propene: A novel strategy to functional (co) poly (a-olefin) s.
Hackmann M, et al.
Macromolecular Chemistry and Physics, 199(8), 1511-1517 (1998)
Qian S Liu et al.
Environmental science & technology, 51(17), 10173-10183 (2017-07-27)
Per- and polyfluoroalkyl substances (PFASs) are a global concern because of their ubiquitous occurrence and high persistence in human blood, and increasing amounts of unidentified fluorinated compounds are now becoming new exposure issues. This study aims to investigate the structure-related
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