추천 제품
Quality Level
분석
98%
refractive index
n20/D 1.429 (lit.)
bp
150 °C (lit.)
mp
−9 °C (lit.)
density
2.474 g/mL at 25 °C (lit.)
SMILES string
FC(F)(I)C(F)(F)C(F)(F)C(F)(F)I
InChI
1S/C4F8I2/c5-1(6,3(9,10)13)2(7,8)4(11,12)14
InChI key
JILAKKYYZPDQBE-UHFFFAOYSA-N
일반 설명
Octafluoro-1,4-diiodobutane (ofib, C4F8I2) is also referred to as 1,1,2,2,3,3,4,4-octafluoro-1,4-diiodobutane. It acts as a halogen bond donor compound and its cocrystallization with methyldiphenylphosphine oxide (mdppo) has been investigated. In combination with a calixcrown compound ofib forms a ′binary host′ system, which is employed for the isolation of cesium iodide from aqueous to fluorous phase.
애플리케이션
Octafluoro-1,4-diiodobutane may be used as a guest molecule to prepare a chiral bidentate inclusion complex with pyridyl moieties of a pyridoallenoacetylenic host. It may be employed in the synthesis of three-component supramolecular complexes.
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
이미 열람한 고객
Switching between halogen-and hydrogen-bonding in stoichiometric variations of a cocrystal of a phosphine oxide.
CrystEngComm, 14(19), 6110-6114 (2012)
Metric engineering of supramolecular Borromean rings.
Chemical Communications (Cambridge, England), 17, 1819-1821 (2006)
Dipyridinocalixcrown/diiodoperfluorocarbon binary host systems for CsI: structural studies and fluorous phase extraction of caesium.
Tetrahedron, 63(23), 4951-4958 (2007)
Organic letters, 16(4), 1136-1139 (2014-02-12)
A chiral bidentate inclusion complex has been formed by halogen-bond interaction between the pyridyl moieties of a pyridoallenoacetylenic host and octafluorodiiodobutane. X-ray crystallography showed that the guest adopts a chiral conformation inside the molecular channels formed by stacking of the
Journal of applied toxicology : JAT, 39(7), 945-954 (2019-03-06)
Fluorinated diiodine alkanes (FDIAs), important industrial intermediates in the synthesis of various perfluorinated compounds, which are distributed widely in wildlife and humans. Recent studies showed that FDIAs had in vitro estrogenic effects. However, to date, little information is available regarding
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