5-Bromo-1,4-dimethyl-1H-1,2,3-triazole
≥95%
- Product Code: 48833
CAS:
1040275-55-5
| Molecular Weight: | 176.02 g./mol | Molecular Formula: | C₄H₆BrN₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14706833 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This chemical is primarily used in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. It is particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and other biologically active compounds. Its triazole ring structure is a key feature that allows it to participate in various chemical reactions, making it a useful building block in drug discovery and development. Additionally, it can be employed in the creation of advanced materials, such as polymers and coatings, due to its ability to introduce specific functional groups into a molecular framework. Researchers also utilize it in the study of chemical reactivity and as a precursor for further modifications in experimental chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | £376.57 |
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5-Bromo-1,4-dimethyl-1H-1,2,3-triazole
This chemical is primarily used in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex molecules. It is particularly valuable in the synthesis of pharmaceuticals, agrochemicals, and other biologically active compounds. Its triazole ring structure is a key feature that allows it to participate in various chemical reactions, making it a useful building block in drug discovery and development. Additionally, it can be employed in the creation of advanced materials, such as polymers and coatings, due to its ability to introduce specific functional groups into a molecular framework. Researchers also utilize it in the study of chemical reactivity and as a precursor for further modifications in experimental chemistry.
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