N,N'-(4,5-difluoro-1,2-phenylene)bis(4-methylbenzenesulfonamide)
95%
- Product Code: 50409
CAS:
335334-08-2
Molecular Weight: | 452.49 g./mol | Molecular Formula: | C₂₀H₁₈F₂N₂O₄S₂ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the development of advanced materials and organic electronics due to its unique structural properties. It serves as a key intermediate in the synthesis of specialized polymers and organic semiconductors, which are essential for manufacturing high-performance electronic devices such as organic light-emitting diodes (OLEDs) and field-effect transistors (FETs). Additionally, its sulfonamide groups make it a valuable component in the design of pharmaceuticals, particularly in the creation of compounds with potential antimicrobial or anti-inflammatory properties. Its fluorinated aromatic structure also contributes to its use in agrochemical research, where it aids in the development of new pesticides and herbicides with enhanced stability and efficacy.
Product Specification:
Test | Specification |
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PURITY | 94.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | £33.99 |
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0.250 | 10-20 days | £57.81 |
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1.000 | 10-20 days | £118.87 |
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N,N'-(4,5-difluoro-1,2-phenylene)bis(4-methylbenzenesulfonamide)
This chemical is primarily utilized in the development of advanced materials and organic electronics due to its unique structural properties. It serves as a key intermediate in the synthesis of specialized polymers and organic semiconductors, which are essential for manufacturing high-performance electronic devices such as organic light-emitting diodes (OLEDs) and field-effect transistors (FETs). Additionally, its sulfonamide groups make it a valuable component in the design of pharmaceuticals, particularly in the creation of compounds with potential antimicrobial or anti-inflammatory properties. Its fluorinated aromatic structure also contributes to its use in agrochemical research, where it aids in the development of new pesticides and herbicides with enhanced stability and efficacy.
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