3,4-DIAMINOCYCLOBUT-3-ENE-1,2-DIONE
98%
- Product Code: 43958
CAS:
5231-89-0
| Molecular Weight: | 112.09 g./mol | Molecular Formula: | C₄H₄N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00205212 | |
| Melting Point: | Boiling Point: | 213.8±50.0℃ at 760 mmHg | |
| Density: | 1.638±0.06 g/cm3 | Storage Condition: | 2-8°C, dry, airtight |
Product Description:
This chemical is primarily utilized in organic synthesis as a building block for creating complex molecules. It is particularly valuable in the development of pharmaceuticals, where it serves as a precursor for compounds with potential therapeutic properties. Its unique structure allows for the formation of heterocyclic compounds, which are often explored for their biological activity. Additionally, it is used in materials science for the synthesis of advanced polymers and coatings, leveraging its reactivity to enhance material properties. Its application in research also extends to the study of reaction mechanisms and the development of novel synthetic routes.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Yellow solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,260.00 |
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| 5.000 | 10-20 days | ฿5,200.00 |
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3,4-DIAMINOCYCLOBUT-3-ENE-1,2-DIONE
This chemical is primarily utilized in organic synthesis as a building block for creating complex molecules. It is particularly valuable in the development of pharmaceuticals, where it serves as a precursor for compounds with potential therapeutic properties. Its unique structure allows for the formation of heterocyclic compounds, which are often explored for their biological activity. Additionally, it is used in materials science for the synthesis of advanced polymers and coatings, leveraging its reactivity to enhance material properties. Its application in research also extends to the study of reaction mechanisms and the development of novel synthetic routes.
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