2,5-Dimethoxybenzaldehyde CAS 93-02-7
2,5-Dimethoxybenzaldehyde CAS 93-02-7, stock available, hot selling in USA, Canada and Europe.
CAS 93-02-7 Basic Parameter
| Product Name | 2,5-Dimethoxybenzaldehyde |
| Synonyms | 2,5-Dimethoxybenzaldehyde,97%;2,5-Dimethoxybenzald;5-DiMethoxybenzaldehyde;;NSC6315;93-02–7;2,5-DimethoxybenzaldehydeVetec(TM)reagentgrade,98%;2,5-DIMETHOXYBENZALDEHYDE |
| CAS NO | 93-02-7 |
| Molecular Formula | C9H10O3 |
| Molecular Weight | 166.17 |
| EINECS | 202-211-5 |
| Melting Point | 46-48 °C (lit.) |
| Boiling Point | 146 °C/10 mmHg (lit.) |
| Flash Point | >230 °F |
| Density | 1.1708 (rough estimate) |
| Storage | Keep in dark place,Sealed in dry,Room Temperature |
| Solubility | Solubility in water is 795 mg/L |
| Form | Crystalline powder, crystal or lump |
| Color | yellow to beige |
| Water Solubility | Soluble in chloroform and methanol. Slightly soluble in water |
2-Phenylacetamide Picture
What is 2,5-Dimethoxybenzaldehyde?
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.
Chemistry
2,5-Dimethoxybenzaldehyde is a key starting material in the synthesis of 2C-B, 2C-I, and 2C-C, which are members of the 2C family of psychedelic drugs. 2,5-Dimethoxybenzaldehyde can undergo a series of chemical reactions to produce the desired final compounds. These reactions typically involve the addition of specific reagents and catalysts. One common method for synthesizing 2C-B from 2,5-Dimethoxybenzaldehyde involves converting 2,5-Dimethoxybenzaldehyde to 2,5-dimethoxyphenethylamine (2C-H) through a reductive amination reaction. 2C-H is then further modified to produce 2C-B. Similarly, 2,5-Dimethoxybenzaldehyde can be used as a precursor to synthesize 2C-I and 2C-C by modifying the chemical structure of 2C-H.
One of the reasons 2,5-Dimethoxybenzaldehyde is chosen as a precursor due to its structural similarity to the target compounds. By modifying specific functional groups on 2,5-Dimethoxybenzaldehyde, it is possible to create the desired psychedelic effects. The synthesis of these compounds typically involves multiple steps and requires careful control of reaction conditions to ensure high yields and purity. The use of 2,5-Dimethoxybenzaldehyde as a precursor allows for the production of these psychedelic drugs in a controlled laboratory setting, ensuring quality and consistency of the final product. The synthesis of 2C-B, 2C-I, and 2C-C from 2,5-Dimethoxybenzaldehyde allows for the exploration of their pharmacological properties and potential therapeutic uses.
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