25480
1-Chloro-3-nitrobenzene
purum, ≥98.0% (GC)
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About This Item
Fórmula linear:
ClC6H4NO2
Número CAS:
Peso molecular:
157.55
Beilstein:
1907947
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
grau
purum
Ensaio
≥98.0% (GC)
pb
236 °C (lit.)
pf
43-47 °C (lit.)
43-47 °C
densidade
1.534 g/mL at 25 °C (lit.)
cadeia de caracteres SMILES
[O-][N+](=O)c1cccc(Cl)c1
InChI
1S/C6H4ClNO2/c7-5-2-1-3-6(4-5)8(9)10/h1-4H
chave InChI
KMAQZIILEGKYQZ-UHFFFAOYSA-N
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[Hygienic study of the stability of methylnitrophos and pentachloronitrobenzene used in agriculture].
Sh T Atabaev et al.
Gigiena i sanitariia, (2)(2), 74-75 (1983-02-01)
Violeta Simic-Milosevic et al.
Angewandte Chemie (International ed. in English), 48(22), 4061-4064 (2009-04-01)
Chirality chameleon: Inelastic electron tunneling manipulation can be used to change a single chloronitrobenzene (ClNB) molecule, randomly adsorbed on Au(111), into its desired enantiomeric form (r or l, see STM images and ball-and-stick representation) and to vary its rotational orientation.
2-Chloronitrobenzene, 3-chloronitrobenzene and 4-chloronitrobenzene.
IARC monographs on the evaluation of carcinogenic risks to humans, 65, 263-296 (1996-01-01)
V Simic-Milosevic et al.
Physical review letters, 98(11), 116102-116102 (2007-05-16)
A scanning tunneling microscope operating at 5 K is used to induce the isomerization of single chloronitrobenzene molecules on Cu(111) and verify the reaction. The threshold voltage of (227+/-7) mV for this reaction is explained based on electron-induced vibrational heating.
Maofa Ge et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 71(4), 1499-1502 (2008-06-25)
The electronic structures and substituent effects of o-, m-, and p-chloronitrobenzene and bromonitrobenzene have been studied by ultraviolet photoelectron spectroscopy (UPS). It was found that the o-isomer possesses particular electronic properties. This characteristic depends on the conjugation between the benzene
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