| 
 | |||
| Names | |||
|---|---|---|---|
| Preferred IUPAC name 4-Nitrobenzaldehyde | |||
| Other names p-Nitrobenzaldehyde | |||
| 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) | |||
| ChEBI | |||
| ChEMBL | |||
| ChemSpider | |||
| ECHA InfoCard | 100.008.259 | ||
| PubChem CID | |||
| UNII | |||
| CompTox Dashboard (EPA) | |||
| 
 | |||
| 
 | |||
| 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). 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.
- ↑ "p-NITROBENZALDEHYDE". Organic Syntheses. 18: 61. 1938. doi:10.15227/orgsyn.018.0061.
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