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CasNo: 555-16-8
MF: C7H5NO3
Appearance: Yellow to brown crystalline powder
Synthesis Reference(s) |
Journal of the American Chemical Society, 78, p. 252, 1956 DOI: 10.1021/ja01582a072Tetrahedron Letters, 28, p. 4285, 1987 DOI: 10.1016/S0040-4039(00)96486-4 |
Purification Methods |
Purify it as for m-nitrobenzaldehyde above. [Beilstein 7 IV 589.] |
Definition |
ChEBI: 4-nitrobenzaldehyde is a C-nitro compound that is benzaldehyde substituted at the para-position with a nitro group. It is a C-nitro compound and a member of benzaldehydes. |
InChI:InChI=1/C7H5NO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-5H
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1-methyl-4-nitrobenzene
acetic anhydride
4-nitrobenzyl chloride
4-nitrobenzyl acetate
4-nitrobenzaldehdye
4-nitrobenzylidene diacetate
1-bromomethyl-4-nitro-benzene
Conditions | Yield |
---|---|
With sulfuric acid; ozone; potassium bromide; manganese(II); In acetic acid; at 10 ℃; for 2h; Rate constant; Product distribution; other catalysts (Co(II), Cr(III) or mixture), other times;;
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42% |
(E)-4,4'-(but-1-ene-1,3-diyl)bis(nitrobenzene)
n-heptane
2-(4-nitrophenyl)propionaldehyde
4-nitrobenzaldehdye
(4-nitrophenyl)ethanone
toluene
Conditions | Yield |
---|---|
With oxygen; In acetonitrile; Mechanism; Irradiation;
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5-methoxy-2-(4-nitro-phenyl)-[1,3]dioxane
pyridine
N-(4-nitrobenzylidene)-1-phenylmethanamine
4-nitrobenzyl chloride
p-Nitrophenyloxirane
1-(4-nitrophenyl)propan-2-one
(4-nitrophenyl)ethanone
(E)-2-methyl-3-(4-nitrophenyl)acrylic acid