5-Amino-1-(tert-butyl)-1H-pyrrole-3-carbonitrile
95%
- Product Code: 48590
CAS:
269726-49-0
| Molecular Weight: | 163.2200 g./mol | Molecular Formula: | C₉H₁₃N₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11846194 | |
| Melting Point: | Boiling Point: | 319.9 °C at 760 mmHg | |
| Density: | 1.04g/cm3 | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various heterocyclic compounds. Its structure, featuring both an amino group and a nitrile group, makes it a versatile building block for the development of pharmaceuticals, agrochemicals, and specialty chemicals. In pharmaceutical research, it is often employed in the synthesis of potential drug candidates, particularly those targeting neurological and inflammatory disorders. Additionally, its application extends to the development of advanced materials, where it contributes to the creation of polymers and coatings with specific functional properties. The tert-butyl group enhances its stability, making it suitable for use in complex synthetic pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,701.00 |
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5-Amino-1-(tert-butyl)-1H-pyrrole-3-carbonitrile
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various heterocyclic compounds. Its structure, featuring both an amino group and a nitrile group, makes it a versatile building block for the development of pharmaceuticals, agrochemicals, and specialty chemicals. In pharmaceutical research, it is often employed in the synthesis of potential drug candidates, particularly those targeting neurological and inflammatory disorders. Additionally, its application extends to the development of advanced materials, where it contributes to the creation of polymers and coatings with specific functional properties. The tert-butyl group enhances its stability, making it suitable for use in complex synthetic pathways.
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