4-Phenyl-1,2,4-triazoline-3,5-dione
97%
- Product Code: 119640
Alias:
PTAD;4-Phenyl-3H-1,2,4-triazole-3,5(4H)-dione
CAS:
4233-33-4
Molecular Weight: | 175.15 g./mol | Molecular Formula: | C₈H₅N₃O₂ |
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EC Number: | 224-191-7 | MDL Number: | MFCD00003148 |
Melting Point: | 165-170 °C (dec.)(lit.) | Boiling Point: | |
Density: | Storage Condition: | 2~8°C |
Product Description:
Used primarily as a dienophile in Diels-Alder reactions, it facilitates the synthesis of complex organic compounds, particularly in the preparation of heterocyclic structures. Its high reactivity makes it valuable in polymer chemistry for cross-linking and modifying polymers to enhance their properties. Additionally, it is employed in organic synthesis to introduce phenyl and triazole groups into molecules, which can be useful in pharmaceutical and agrochemical research. The compound is also utilized in the study of reaction mechanisms due to its distinct reactivity pattern.
Product Specification:
Test | Specification |
---|---|
Carbon | 52.9-56.8 |
Nitrogen | 23.5-24.3 |
Purity (HPLC) | 97-100 |
Appearance | RED TO RED-ORANGE OR RED-PINK POWDER OR CRYSTALS |
Infrared Spectrum | Conforms To Structure |
NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | ฿480.00 |
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1.000 | 10-20 days | ฿1,060.00 |
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5.000 | 10-20 days | ฿4,350.00 |
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25.000 | 10-20 days | ฿15,440.00 |
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100.000 | 10-20 days | ฿53,400.00 |
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4-Phenyl-1,2,4-triazoline-3,5-dione
Used primarily as a dienophile in Diels-Alder reactions, it facilitates the synthesis of complex organic compounds, particularly in the preparation of heterocyclic structures. Its high reactivity makes it valuable in polymer chemistry for cross-linking and modifying polymers to enhance their properties. Additionally, it is employed in organic synthesis to introduce phenyl and triazole groups into molecules, which can be useful in pharmaceutical and agrochemical research. The compound is also utilized in the study of reaction mechanisms due to its distinct reactivity pattern.
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