219428
4-Fluoroiodobenzene
99%
동의어(들):
1-Fluoro-4-iodobenzene, 1-Iodo-4-fluorobenzene, 4-Fluoro-1-iodobenzene, 4-Fluorophenyl iodide, 4-Iodo-1-fluorobenzene, 4-Iodofluorobenzene, p-Fluoroiodobenzene, p-Fluorophenyl iodide, p-Iodofluorobenzene
로그인조직 및 계약 가격 보기
모든 사진(1)
About This Item
Linear Formula:
FC6H4I
CAS Number:
Molecular Weight:
222.00
EC Number:
MDL number:
UNSPSC 코드:
12352100
PubChem Substance ID:
NACRES:
NA.22
추천 제품
Quality Level
분석
99%
양식
liquid
포함
copper as stabilizer
refractive index
n20/D 1.583 (lit.)
bp
182-184 °C (lit.)
mp
−20 °C (lit.)
density
1.925 g/mL at 25 °C (lit.)
작용기
fluoro
iodo
SMILES string
Fc1ccc(I)cc1
InChI
1S/C6H4FI/c7-5-1-3-6(8)4-2-5/h1-4H
InChI key
KGNQDBQYEBMPFZ-UHFFFAOYSA-N
일반 설명
4-[18F] Fluoroiodobenzene is a versatile building block in 18F radiochemistry and is used in various transition metal-mediated C-C and C-N cross-coupling reactions. Cross-coupling reaction of 4-fluoroiodobenzene with potassium pentafluorophenyltrifluoroborate in the presence of different palladium catalysts and silver oxide in toluene has been investigated.
애플리케이션
4-Fluoroiodobenzene was used in the preparation of fluorotriphenylene derivatives.
신호어
Warning
유해 및 위험 성명서
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
표적 기관
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
154.4 °F - closed cup
Flash Point (°C)
68 °C - closed cup
개인 보호 장비
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
이미 열람한 고객
Jenilee Dawn Way et al.
Journal of labelled compounds & radiopharmaceuticals, 57(2), 104-109 (2014-03-29)
4-[18F]Fluoroiodobenzene ([18F]FIB) is a versatile building block in 18F radiochemistry used in various transition metal-mediated C-C and C-N cross-coupling reactions and [18F]fluoroarylation reactions. Various synthesis routes have been described for the preparation of [18F]FIB. However, to date, no automated synthesis
The effect of N-heterocyclic carbene ligands in the palladium-catalyzed cross-coupling reaction of K [C6F5BF3] with aryl iodides and aryl bromides.
Adonin NY, et al.
Tetrahedron, 64(25), 5920-5924 (2008)
Thiruvellore Thatai Jayanth et al.
Chemical communications (Cambridge, England), (8)(8), 894-896 (2006-02-16)
Highly substituted triphenylene derivatives were prepared in good yields via the palladium-catalyzed carbocyclization of arynes with aryl iodides.
Gabriel A Odugbesi et al.
Journal of chromatography. A, 1604, 460466-460466 (2019-09-03)
Ionic liquids (ILs) are well-known in the field of separation science for their unique selectivity when used as stationary phases in gas chromatography (GC). While a significant amount of knowledge has been attained in correlating structural features of an IL
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