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化驗
99%
形狀
liquid
折射率
n20/D 1.532 (lit.)
bp
116 °C/22 mmHg (lit.)
mp
−9-−6 °C (lit.)
密度
1.338 g/mL at 25 °C (lit.)
SMILES 字串
[O-][N+](=O)c1ccccc1F
InChI
1S/C6H4FNO2/c7-5-3-1-2-4-6(5)8(9)10/h1-4H
InChI 密鑰
PWKNBLFSJAVFAB-UHFFFAOYSA-N
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訊號詞
Danger
危險分類
Acute Tox. 3 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Aquatic Chronic 2 - STOT RE 1
儲存類別代碼
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
水污染物質分類（WGK）
WGK 3
閃點（°F）
201.2 °F - closed cup
閃點（°C）
94 °C - closed cup
個人防護裝備
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
V Arjunan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 84(1), 196-209 (2011-10-14)
Experimental FTIR, FT-Raman and FT-NMR spectroscopic studies of o-fluoronitrobenzene and p-fluoronitrobenzene have been carried out. A detailed quantum chemical calculations have been performed using DFT/B3LYP method with 6-311++G** and 6-31G** basis sets. Complete vibrational analyses of the compounds were performed.
N Tuset et al.
Allergologia et immunopathologia, 14(6), 489-497 (1986-11-01)
The multi-functionality of a given antibody, even monoclonal antibody has recently been shown; this raises the possibility that the specificity of an antiserum be due to a population phenomena; i.e., the specificity would be the net result of the affinity
V Udayakumar et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 83(1), 575-586 (2011-10-01)
FT-IR and FT-Raman spectra of p-fluoronitrobenzene (FNO(2)C(6)H(4)) have been recorded in the region 4000-100 cm(-1). In this work, the experimental and theoretical spectra of p-fluoronitrobenzene (p-FNBz) are studied. The molecular geometry and vibrational frequencies are calculated in the ground state
Kathryn E O'Harra et al.
Membranes, 9(7) (2019-07-07)
Three new isomeric 6FDA-based polyimide-ionenes, with imidazolium moieties and varying regiochemistry (para-, meta-, and ortho- connectivity), and composites with three different ionic liquids (ILs) have been developed as gas separation membranes. The structural-property relationships and gas separation behaviors of the
Krishnananda Samanta et al.
Organic & biomolecular chemistry, 8(12), 2823-2828 (2010-04-24)
A new series of enantiomerically pure 2,3,4,4a,5,6-hexahydro-1H-pyrazino[1,2-a]quinoxalines were synthesized for the first time in twelve steps from 1-fluoro-2-nitrobenzene and S-amino acids with 13-20% overall yields. First use of intramolecular Mitsunobu cyclization for 1,2,3,4-tetrahydroquinoxalines followed by PPh(3)/I(2)/imidazole mediated 6-exo-tet cyclization were
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