4-Nitrobenzaldehyde
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| Names | |||
|---|---|---|---|
| IUPAC name
4-Nitrobenzaldehyde | |||
| Other names
p-Nitrobenzaldehyde | |||
| Properties | |||
| C7H5NO3 | |||
| Molar mass | 151.12 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] | ||
| Identifiers | |||
555-16-8  | |||
| 3D model (Jmol) | Interactive image | ||
| ChEBI | CHEBI:66926  | ||
| ChEMBL | ChEMBL164236 | ||
| ChemSpider | 526 | ||
| ECHA InfoCard | 100.008.259 | ||
| PubChem | 541 | ||
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| Hazards | |||
| GHS pictograms |  [2] | ||
| H317, H319 | |||
| P280, P305+351+338 | |||
| R-phrases | R36 R43 R52/53 | ||
| S-phrases | S26 S36/37 S61 | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
| verify (what is ?) | |||
| Infobox references | |||
4-Nitrobenzaldehyde is an organic aromatic compound containing a nitro group para-substituted to an aldehyde.
Nitrobenzyldiacetate is obtained by the reaction of 4-nitrotoluene and chromium(VI) oxide in acetic anhydride. 4-Nitrobenzaldehyde is obtained by hydrolysis by sulfuric acid in ethanol.[3]
References
- 1 2 4-Nitrobenzaldehyde(555-16-8) (Date Accessed 17 April 2013)
- 1 2 Sigma-Aldrich Co., 4-Nitrobenzaldehyde. Retrieved on 4 May 2011.
- ↑ 4-Nitrobenzaldehyd, Versuchsvorschrift aus: Organic Syntheses, Coll. Vol. 2, p. 441 (1943); Vol. 18, p. 61 (1938).
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