4-Methylbenzaldehyde
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| Names | |||
|---|---|---|---|
| IUPAC name
4-methylbenzaldehyde | |||
| Other names
p-Tolualdehyde; p-tolylaldehyde | |||
| Identifiers | |||
| 104-87-0 | |||
| ChEBI | CHEBI:28617 | ||
| ChEMBL | ChEMBL190927 | ||
| ChemSpider | 13865424 | ||
| Jmol interactive 3D | Image Image | ||
| KEGG | C06758 | ||
| PubChem | 7725 | ||
| UNII | GAX22QZ28Q | ||
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| Properties | |||
| C8H8O | |||
| Molar mass | 120.14852 | ||
| Appearance | colorless liquid | ||
| Density | 1.019 g/mL (25 °C) | ||
| Melting point | −6.00 °C (21.20 °F; 267.15 K) | ||
| Boiling point | 204 to 205 °C (399 to 401 °F; 477 to 478 K) | ||
| Refractive index (nD) |
1.545 (20 °C) | ||
| Hazards | |||
| Safety data sheet | Aldrich MSDS, reprinted | ||
| Related compounds | |||
| Related compounds |
Benzaldehyde | ||
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |||
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| Infobox references | |||
4-Methylbenzaldehyde is a simple aromatic aldehyde. It is commercially available, but may be prepared from the Friedel-Crafts formylation of toluene with carbon monoxide and hydrogen chloride under Gattermann-Koch conditions:.[1] 4-Methylbenzaldehyde has a cherry-like scent similar to benzaldehyde.
References
- ↑ G. H. Coleman, David Craig (1943). "p-Tolualdehyde". Org. Synth.; Coll. Vol. 2, p. 583
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