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]
Quick facts Names, Identifiers ...
2,5-Dimethoxybenzaldehyde
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| Names |
Preferred IUPAC name
2,5-Dimethoxybenzaldehyde |
| Identifiers |
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| ChemSpider |
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| ECHA InfoCard |
100.002.011 |
| EC Number |
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| UNII |
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InChI=1S/C9H10O3/c1-11-8-3-4-9(12-2)7(5-8)6-10/h3-6H,1-2H3 Y Key: AFUKNJHPZAVHGQ-UHFFFAOYSA-N Y InChI=1/C9H10O3/c1-11-8-3-4-9(12-2)7(5-8)6-10/h3-6H,1-2H3 Key: AFUKNJHPZAVHGQ-UHFFFAOYAN
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| Properties |
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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 |
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H315, H319, H334, H335 |
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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) |
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| 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).
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