4-Bromo-3,5-dimethylisoxazole
>98.0%(GC)
- Product Code: 119323
Alias:
3,5-Dimethyl-4-bromoisoxazole
4-Bromo-3,5-dimethylethyl ester
CAS:
10558-25-5
| Molecular Weight: | 176.01 g./mol | Molecular Formula: | C₅H₆BrNO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00068187 | |
| Melting Point: | Boiling Point: | 176 °C(lit.) | |
| Density: | 1.478 g/mL at 25 °C(lit.) | Storage Condition: | 2~8°C |
Product Description:
Used primarily as an intermediate in organic synthesis, this compound plays a crucial role in the development of pharmaceuticals and agrochemicals. Its structure allows for the introduction of bromine into more complex molecules, facilitating the creation of compounds with potential biological activity. In medicinal chemistry, it serves as a building block for the synthesis of various drugs, particularly those targeting neurological and infectious diseases. Additionally, it is employed in research settings to study chemical reactions and mechanisms involving halogenated heterocycles, aiding in the discovery of new chemical entities.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 98 |
| Refractive Index N20/D | 1.488-1.492 |
| Specific Gravity (20/20 Degree Celsius) | 1.539-1.544 |
| Appearance | Colorless To Brown Liquid |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $13.06 |
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| 5.000 | 10-20 days | $33.15 |
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| 25.000 | 10-20 days | $97.44 |
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| 100.000 | 10-20 days | $237.07 |
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4-Bromo-3,5-dimethylisoxazole
Used primarily as an intermediate in organic synthesis, this compound plays a crucial role in the development of pharmaceuticals and agrochemicals. Its structure allows for the introduction of bromine into more complex molecules, facilitating the creation of compounds with potential biological activity. In medicinal chemistry, it serves as a building block for the synthesis of various drugs, particularly those targeting neurological and infectious diseases. Additionally, it is employed in research settings to study chemical reactions and mechanisms involving halogenated heterocycles, aiding in the discovery of new chemical entities.
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