assay
99%
mp
75-77 °C (lit.)
functional group
fluoro, nitro
SMILES string
Oc1ccc(F)cc1[N+]([O-])=O
InChI
1S/C6H4FNO3/c7-4-1-2-6(9)5(3-4)8(10)11/h1-3,9H
InChI key
ZHRLVDHMIJDWSS-UHFFFAOYSA-N
General description
4-Fluoro-2-nitrophenol is formed during iron(III) nitrate nonahydrate activated by tungstophosphoric acid cesium salt catalyzed nitration of 4-fluorophenol.
Application
4-Fluoro-2-nitrophenol may be used in the preparation of 5-fluoro-2-methoxyanilineand 5-fluoro-2-hydroxyaniline.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
SOME SYNTHESES FROM p-FLUOROANISOLE.
BUU-HOI NP, et al.
The Journal of Organic Chemistry, 19(10), 1617-1621 (1954)
I M Rietjens et al.
European journal of biochemistry, 194(3), 945-954 (1990-12-27)
Pathways for biodehalogenation of fluorinated aniline derivatives were investigated. Microsomal NADPH-dependent dehalogenation of fluoroanilines was shown to proceed by three different reaction pathways. The first route appeared to result in monooxygenation at a fluorinated position and release of the fluorine
Catalytic effects of some Keggin-type heteropoly acids and polyoxometalates on selective nitration of phenols.
Amani K and Maleki F.
Journal of the Iranian Chemical Society, 4(2), 238-243 (2007)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 345059-5G | 04061832279923 |
| 345059-25G | 04061832279916 |