4-Nitrobenzaldehyde
Appearance
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Names | |||
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Preferred IUPAC name
4-Nitrobenzaldehyde | |||
Other names
p-Nitrobenzaldehyde
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Properties | |||
C7H5NO3 | |||
Molar mass | 151.121 g·mol−1 | ||
Appearance | slightly yellowish crystalline powder | ||
Density | 1.546 g/cm3[1] | ||
Melting point | 103 to 106 °C (217 to 223 °F; 376 to 379 K)[2] | ||
Boiling point | 300 °C (572 °F; 573 K)[1] | ||
-66.57·10−6 cm3/mol | |||
Identifiers | |||
3D model (JSmol)
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ChEBI | |||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.008.259 | ||
PubChem CID
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UNII | |||
CompTox Dashboard (EPA)
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Hazards | |||
GHS labelling: | |||
[2] | |||
H317, H319 | |||
P280, P305+P351+P338 | |||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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4-Nitrobenzaldehyde is an organic compound with the formula O2NC6H4CHO. It is one of three isomers of nitrobenzaldehyde. It contains a nitro group para-substituted to an aldehyde.
4-Nitrobenzaldehyde is obtained by oxidation of 4-nitrotoluene or hydrolysis of 4-nitrobenzalbromide:[3]
- O2NC6H4CHBr2 + H2O → O2NC6H4CHO + 2 HBr
In the laboratory, the oxidation is achieved with chromium(VI) oxide in acetic anhydride, which affords nitrobenzyldiacetate.[4]
References
[edit]- ^ a b 4-Nitrobenzaldehyde(555-16-8) (Date Accessed 17 April 2013)
- ^ a b Sigma-Aldrich Co., 4-Nitrobenzaldehyde. Retrieved on 4 May 2011.
- ^ Brühne, Friedrich; Wright, Elaine (2011). "Benzaldehyde". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a03_463.pub2. ISBN 978-3-527-30385-4.
- ^ Lieberman, S. V.; Connor, Ralph (1938). "p-Nitrobenzaldehyde". Organic Syntheses. 18: 61. doi:10.15227/orgsyn.018.0061.