4-Bromo-2,5-dimethyl-2H-1,2,3-triazole
97%
- Product Code: 119250
CAS:
942060-54-0
| Molecular Weight: | 176.01 g./mol | Molecular Formula: | C₄H₆BrN₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14706834 | |
| Melting Point: | Boiling Point: | 244°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily used in the field of organic synthesis as a versatile building block for the development of more complex molecules. It serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for the introduction of functional groups, enabling the creation of compounds with specific biological or chemical properties. Additionally, it is employed in research and development for the synthesis of novel triazole derivatives, which are often explored for their potential therapeutic applications, including antimicrobial, antifungal, and anticancer activities. Its role in click chemistry reactions further enhances its utility in creating diverse molecular architectures for industrial and academic purposes.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Colorless To Pale-yellow To Yellow-brown Liquid |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿5,200.00 |
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| 0.250 | 10-20 days | ฿8,490.00 |
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| 1.000 | 10-20 days | ฿26,470.00 |
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4-Bromo-2,5-dimethyl-2H-1,2,3-triazole
This chemical is primarily used in the field of organic synthesis as a versatile building block for the development of more complex molecules. It serves as a key intermediate in the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its unique structure allows for the introduction of functional groups, enabling the creation of compounds with specific biological or chemical properties. Additionally, it is employed in research and development for the synthesis of novel triazole derivatives, which are often explored for their potential therapeutic applications, including antimicrobial, antifungal, and anticancer activities. Its role in click chemistry reactions further enhances its utility in creating diverse molecular architectures for industrial and academic purposes.
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