Diphenyl selenide
98%
- Product Code: 86208
CAS:
1132-39-4
Molecular Weight: | 233.17 g./mol | Molecular Formula: | C₁₂H₁₀Se |
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EC Number: | 14-474-2 | MDL Number: | MFCD00014067 |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | Room temperature, airtight, dry |
Product Description:
Diphenyl selenide is primarily used in organic synthesis as a reagent or catalyst. It plays a role in the formation of carbon-selenium bonds, which are valuable in various chemical reactions, including the synthesis of organoselenium compounds. These compounds are useful in materials science, particularly in the development of semiconductors and photovoltaic materials. Additionally, diphenyl selenide is employed in the preparation of selenium-containing polymers, which exhibit unique properties like thermal stability and electrical conductivity. It also finds application in medicinal chemistry for the synthesis of selenium-based drugs, which are explored for their antioxidant and anticancer properties.
Product Specification:
Test | Specification |
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APPEARANCE | Clear Colorless to Pale yellow to Orange to Red to Brown-Yellow to Brown Liquid |
PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
REFRACTIVE INDEXN20D | 1.6470-1.6510 |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.200 | 10-20 days | ฿1,680.00 |
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1.000 | 10-20 days | ฿3,060.00 |
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5.000 | 10-20 days | ฿12,420.00 |
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Diphenyl selenide
Diphenyl selenide is primarily used in organic synthesis as a reagent or catalyst. It plays a role in the formation of carbon-selenium bonds, which are valuable in various chemical reactions, including the synthesis of organoselenium compounds. These compounds are useful in materials science, particularly in the development of semiconductors and photovoltaic materials. Additionally, diphenyl selenide is employed in the preparation of selenium-containing polymers, which exhibit unique properties like thermal stability and electrical conductivity. It also finds application in medicinal chemistry for the synthesis of selenium-based drugs, which are explored for their antioxidant and anticancer properties.
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