(S)-2-Hydroxy-2-(3-phenoxyphenyl)acetonitrile
95% containing less than 10% EA
- Product Code: 80502
CAS:
61826-76-4
| Molecular Weight: | 225.24 g./mol | Molecular Formula: | C₁₄H₁₁NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01937336 | |
| Melting Point: | Boiling Point: | 399.828°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, airtight, dry |
Product Description:
This chemical is primarily utilized in the synthesis of chiral intermediates for pharmaceuticals, particularly in the production of enantiomerically pure compounds. It serves as a key building block in the development of active pharmaceutical ingredients (APIs) for drugs targeting neurological and inflammatory disorders. Additionally, it is employed in agrochemical research for creating pesticides and herbicides with enhanced efficacy and selectivity. Its chiral nature makes it valuable in asymmetric synthesis, enabling the production of compounds with specific stereochemical configurations required for biological activity.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Light yellow to light red to yellow liquid |
| Puritycontaining less than 10 EA | 94.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿1,050.00 |
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| 25.000 | 10-20 days | ฿4,680.00 |
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(S)-2-Hydroxy-2-(3-phenoxyphenyl)acetonitrile
This chemical is primarily utilized in the synthesis of chiral intermediates for pharmaceuticals, particularly in the production of enantiomerically pure compounds. It serves as a key building block in the development of active pharmaceutical ingredients (APIs) for drugs targeting neurological and inflammatory disorders. Additionally, it is employed in agrochemical research for creating pesticides and herbicides with enhanced efficacy and selectivity. Its chiral nature makes it valuable in asymmetric synthesis, enabling the production of compounds with specific stereochemical configurations required for biological activity.
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