3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chloride
98%
- Product Code: 68504
Alias:
3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chloride; 3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazoline chloride
CAS:
4568-71-2
| Molecular Weight: | 269.79 g./mol | Molecular Formula: | C₁₃H₁₆ClNOS |
|---|---|---|---|
| EC Number: | 224-947-6 | MDL Number: | MFCD00011959 |
| Melting Point: | 142-144 °C(lit.) | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a catalyst, particularly in the formation of carbon-carbon bonds. It is effective in promoting various condensation reactions, such as the benzoin condensation, where it facilitates the coupling of aldehydes to form α-hydroxy ketones. Its thiazolium structure makes it a key component in enzymatic-like processes, mimicking the activity of thiamine (vitamin B1) in biological systems. Additionally, it is employed in the synthesis of heterocyclic compounds, which are valuable in pharmaceutical and agrochemical industries. Its ability to act as a nucleophilic catalyst also makes it useful in the preparation of intermediates for complex organic molecules.
Product Specification:
| Test | Specification |
|---|---|
| Melting point | 142-145 |
| PURITYNONAQUEOUS TIERATION | 97.5-102.5 |
| APPEARANCE | WHITE TO LIGHT ORANGE POWDER,CRYSTALS AND/OR CHUNK |
| INFRARED SPECTRUM | Conforms to Structure |
| SOLUBILITY IN WATER | 0.1g10mlColorless and clear |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿300.00 |
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| 25.000 | 10-20 days | ฿990.00 |
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| 100.000 | 10-20 days | ฿3,720.00 |
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3-Benzyl-5-(2-hydroxyethyl)-4-methylthiazolium chloride
This compound is primarily utilized in organic synthesis as a catalyst, particularly in the formation of carbon-carbon bonds. It is effective in promoting various condensation reactions, such as the benzoin condensation, where it facilitates the coupling of aldehydes to form α-hydroxy ketones. Its thiazolium structure makes it a key component in enzymatic-like processes, mimicking the activity of thiamine (vitamin B1) in biological systems. Additionally, it is employed in the synthesis of heterocyclic compounds, which are valuable in pharmaceutical and agrochemical industries. Its ability to act as a nucleophilic catalyst also makes it useful in the preparation of intermediates for complex organic molecules.
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