(4-Nitrophenyl)(phenyl)sulfane
98%
- Product Code: 87534
CAS:
952-97-6
Molecular Weight: | 231.27 g./mol | Molecular Formula: | C₁₂H₉NO₂S |
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EC Number: | MDL Number: | MFCD00024700 | |
Melting Point: | Boiling Point: | 396.8 °C at 760 mmHg | |
Density: | Storage Condition: | 2-8°C, protected from light, dry, sealed |
Product Description:
(4-Nitrophenyl)(phenyl)sulfane is primarily utilized in organic synthesis as an intermediate for the preparation of more complex chemical compounds. It is often employed in the development of pharmaceuticals, where it serves as a building block for active pharmaceutical ingredients (APIs). Additionally, this compound is used in material science for the synthesis of advanced materials, including polymers and coatings, due to its ability to introduce specific functional groups into the molecular structure. In research, it is a valuable reagent for studying sulfane derivatives and their reactivity, contributing to advancements in chemical synthesis methodologies. Its nitro group makes it particularly useful in reactions involving nucleophilic substitution, enabling the creation of diverse chemical entities.
Product Specification:
Test | Specification |
---|---|
APPEARANCE | Light yellow to Yellow to Brown Crystals or Powder or Crystalline powder |
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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1.000 | 10-20 days | ฿680.00 |
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5.000 | 10-20 days | ฿2,390.00 |
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25.000 | 10-20 days | ฿10,500.00 |
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(4-Nitrophenyl)(phenyl)sulfane
(4-Nitrophenyl)(phenyl)sulfane is primarily utilized in organic synthesis as an intermediate for the preparation of more complex chemical compounds. It is often employed in the development of pharmaceuticals, where it serves as a building block for active pharmaceutical ingredients (APIs). Additionally, this compound is used in material science for the synthesis of advanced materials, including polymers and coatings, due to its ability to introduce specific functional groups into the molecular structure. In research, it is a valuable reagent for studying sulfane derivatives and their reactivity, contributing to advancements in chemical synthesis methodologies. Its nitro group makes it particularly useful in reactions involving nucleophilic substitution, enabling the creation of diverse chemical entities.
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