2,5-Dimethoxybenzaldehyde
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| Names | |
|---|---|
| Preferred IUPAC name 2,5-Dimethoxybenzaldehyde | |
| Identifiers | |
3D model (JSmol) | |
| ChemSpider | |
| ECHA InfoCard | 100.002.011 |
| EC Number |
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PubChem CID | |
| UNII | |
CompTox Dashboard (EPA) | |
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| Properties | |
| C9H10O3 | |
| Molar mass | 166.17 g/mol |
| Appearance | Yellow crystalline solid |
| Density | 1.114 g/mL |
| Melting point | 50 °C (122 °F; 323 K) |
| Boiling point | 283.8 °C (542.8 °F; 557.0 K) |
| Hazards[1] | |
| Occupational safety and health (OHS/OSH): | |
Main hazards | Irritant |
| GHS labelling: | |
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| Danger | |
| H315, H319, H334, H335 | |
| P261, P264, P271, P280, P285, P302+P352, P304+P340, P304+P341, P305+P351+P338, P312, P332+P313, P337+P313, P342+P311, P362, P403+P233, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | 110 °C (230 °F; 383 K) (c.c.) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
2,5-Dimethoxybenzaldehyde is an organic compound and a benzaldehyde derivative. One of its uses is the production of 2,5-dimethoxyphenethylamine, also known as 2C-H. 2C-H is used to produce many other substituted phenethylamines such as 2C-B, 2C-I and 2C-C.[2]
References
- ^ "2,5-Dimethoxybenzaldehyde". pubchem.ncbi.nlm.nih.gov.
- ^ Shulgin, Alexander; Shulgin, Ann (September 1991). PiHKAL: A Chemical Love Story. Berkeley, California: Transform Press. ISBN 0-9630096-0-5. OCLC 25627628.




