1-(4-(Chloromethyl)phenyl)-1H-1,2,3-triazole
97%
- Product Code: 39405
CAS:
1341039-29-9
| Molecular Weight: | 193.6329 g./mol | Molecular Formula: | C₉H₈ClN₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30185155 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a chloromethyl group and a triazole ring, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and functional materials. The chloromethyl group allows for further functionalization through nucleophilic substitution reactions, while the triazole ring contributes to the compound's stability and potential biological activity. It is often employed in click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), to create triazole-linked compounds with applications in drug discovery, polymer chemistry, and bioconjugation. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds, which are essential in designing active pharmaceutical ingredients (APIs) and other biologically relevant molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,527.00 |
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1-(4-(Chloromethyl)phenyl)-1H-1,2,3-triazole
This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. Its structure, featuring a chloromethyl group and a triazole ring, makes it a valuable intermediate in the preparation of pharmaceuticals, agrochemicals, and functional materials. The chloromethyl group allows for further functionalization through nucleophilic substitution reactions, while the triazole ring contributes to the compound's stability and potential biological activity. It is often employed in click chemistry reactions, particularly copper-catalyzed azide-alkyne cycloaddition (CuAAC), to create triazole-linked compounds with applications in drug discovery, polymer chemistry, and bioconjugation. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds, which are essential in designing active pharmaceutical ingredients (APIs) and other biologically relevant molecules.
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