2,5-dimethoxyterephthalohydrazide
98%
- Product Code: 43831
CAS:
114503-42-3
Molecular Weight: | 254.24 g./mol | Molecular Formula: | C₁₀H₁₄N₄O₄ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | 1.320±0.06g/ml(Predicted) | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
2,5-dimethoxyterephthalohydrazide is primarily utilized in the field of organic synthesis and material science. It serves as a key intermediate in the production of specialized polymers and dyes, particularly those requiring precise structural properties. Its hydrazide group enables it to participate in condensation reactions, making it valuable for creating high-performance materials like liquid crystals and photoresists. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to form stable complexes with metal ions, aiding in detection and analytical applications. Its methoxy groups further enhance its solubility and reactivity in various organic solvents, broadening its utility in research and industrial processes.
Product Specification:
Test | Specification |
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APPEARANCE | White to off-white Solid |
PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
NMR | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.250 | 10-20 days | $87.31 |
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1.000 | 10-20 days | $331.83 |
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2,5-dimethoxyterephthalohydrazide
2,5-dimethoxyterephthalohydrazide is primarily utilized in the field of organic synthesis and material science. It serves as a key intermediate in the production of specialized polymers and dyes, particularly those requiring precise structural properties. Its hydrazide group enables it to participate in condensation reactions, making it valuable for creating high-performance materials like liquid crystals and photoresists. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to form stable complexes with metal ions, aiding in detection and analytical applications. Its methoxy groups further enhance its solubility and reactivity in various organic solvents, broadening its utility in research and industrial processes.
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