2,5-Dimethyloxazole-4-carbaldehyde
98%
- Product Code: 55876
CAS:
92901-88-7
| Molecular Weight: | 125.1300 g./mol | Molecular Formula: | C₆H₇NO₂ |
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| EC Number: | MDL Number: | MFCD03923827 | |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
2,5-Dimethyloxazole-4-carbaldehyde is primarily utilized in organic synthesis as a versatile building block for the creation of more complex chemical structures. Its aldehyde functional group makes it a key intermediate in the production of pharmaceuticals, particularly in the synthesis of heterocyclic compounds that exhibit biological activity. Additionally, it is employed in the development of agrochemicals, where it contributes to the formation of active ingredients in pesticides and herbicides. The compound is also explored in material science for the design of organic electronic materials, such as semiconductors and light-emitting diodes (LEDs), due to its ability to participate in condensation reactions and form conjugated systems. Its role in research and development extends to the synthesis of novel dyes and pigments, where its reactivity and structural properties are leveraged to achieve desired color and stability characteristics.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $192.80 |
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2,5-Dimethyloxazole-4-carbaldehyde
2,5-Dimethyloxazole-4-carbaldehyde is primarily utilized in organic synthesis as a versatile building block for the creation of more complex chemical structures. Its aldehyde functional group makes it a key intermediate in the production of pharmaceuticals, particularly in the synthesis of heterocyclic compounds that exhibit biological activity. Additionally, it is employed in the development of agrochemicals, where it contributes to the formation of active ingredients in pesticides and herbicides. The compound is also explored in material science for the design of organic electronic materials, such as semiconductors and light-emitting diodes (LEDs), due to its ability to participate in condensation reactions and form conjugated systems. Its role in research and development extends to the synthesis of novel dyes and pigments, where its reactivity and structural properties are leveraged to achieve desired color and stability characteristics.
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