Di(alpha-phenylethyl) Sulfide
55%, a mixture of racemic and meso
- Product Code: 86201
CAS:
838-59-5
| Molecular Weight: | 242.38 g./mol | Molecular Formula: | C₁₆H₁₈S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00026342 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
Di(alpha-phenylethyl) sulfide is primarily utilized in organic synthesis as a building block or intermediate for the preparation of more complex chemical compounds. Its structure, featuring sulfur and phenyl groups, makes it valuable in the development of ligands for catalytic systems, particularly in asymmetric synthesis where chiral molecules are required. It can also serve as a precursor in the synthesis of sulfur-containing polymers or materials with specific optical or electronic properties. Additionally, it may find applications in the pharmaceutical industry for the creation of novel drug candidates, leveraging its unique chemical framework. Its role in research and development often focuses on exploring new reactions or pathways in organic chemistry.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Almost white to yellow clear liquid |
| Puritytotal of isomers | 55 % |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $112.08 |
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Di(alpha-phenylethyl) Sulfide
Di(alpha-phenylethyl) sulfide is primarily utilized in organic synthesis as a building block or intermediate for the preparation of more complex chemical compounds. Its structure, featuring sulfur and phenyl groups, makes it valuable in the development of ligands for catalytic systems, particularly in asymmetric synthesis where chiral molecules are required. It can also serve as a precursor in the synthesis of sulfur-containing polymers or materials with specific optical or electronic properties. Additionally, it may find applications in the pharmaceutical industry for the creation of novel drug candidates, leveraging its unique chemical framework. Its role in research and development often focuses on exploring new reactions or pathways in organic chemistry.
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