2,5-dimethoxybenzaldehyde
Structural formula | |||||||||||||||||||
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General | |||||||||||||||||||
Surname | 2,5-dimethoxybenzaldehyde | ||||||||||||||||||
Molecular formula | C 9 H 10 O 3 | ||||||||||||||||||
Brief description |
yellow crystalline solid |
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properties | |||||||||||||||||||
Molar mass | 166.17 g mol −1 | ||||||||||||||||||
Physical state |
firmly |
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Melting point |
46-48 ° C |
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boiling point |
146 ° C (10 mmHg ) |
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safety instructions | |||||||||||||||||||
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Toxicological data | |||||||||||||||||||
As far as possible and customary, SI units are used. Unless otherwise noted, the data given apply to standard conditions . |
2,5-Dimethoxybenzaldehyde is an aromatic organic compound and a derivative of benzaldehyde . Among other things, it serves as a starting material for the synthesis of differently substituted phenylethylamines such as 2C-B .
presentation
2,5-Dimethoxybenzaldehyde can be produced in a Vilsmeier-Haack reaction of 1,4-dimethoxybenzene with phosphorus oxychloride and N -methylformamide .
Individual evidence
- ↑ a b c d e f data sheet 2,5-dimethoxybenzaldehyde from Sigma-Aldrich , accessed on November 28, 2019 ( PDF ).
- ^ Daniel Trachsel: Psychedelic Chemistry: Aspects of Psychoactive Molecules , 5th Edition, Nachtschatten Verlag, 2016, ISBN 978-3-90708053-5 .