(S)-()-N-(3,5-DINITROBENZOYL)-ALPHA-PHENYLGLYCINE
98%
- Product Code: 59247
CAS:
90761-62-9
| Molecular Weight: | 345.26 g./mol | Molecular Formula: | C₁₅H₁₁N₃O₇ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00064470 | |
| Melting Point: | 218-220 ℃ | Boiling Point: | 569.4±50.0 ℃ at 760 mmHg |
| Density: | 1.527±0.06 g/cm3 | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as a chiral resolving agent in the separation of enantiomers in organic synthesis. It is particularly effective in forming diastereomeric salts with racemic mixtures, allowing for the purification of optically active compounds. Its application is crucial in the pharmaceutical industry, where the production of single-enantiomer drugs is often necessary to ensure efficacy and reduce side effects. Additionally, it serves as a valuable tool in research laboratories for studying stereochemistry and developing chiral catalysts. Its high enantioselectivity makes it a preferred choice for resolving complex organic molecules.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-White Powder, Crystals, Crystalline Powder and/or Chunks |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | £47.04 |
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| 5.000 | 10-20 days | £164.20 |
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(S)-()-N-(3,5-DINITROBENZOYL)-ALPHA-PHENYLGLYCINE
This chemical is primarily used as a chiral resolving agent in the separation of enantiomers in organic synthesis. It is particularly effective in forming diastereomeric salts with racemic mixtures, allowing for the purification of optically active compounds. Its application is crucial in the pharmaceutical industry, where the production of single-enantiomer drugs is often necessary to ensure efficacy and reduce side effects. Additionally, it serves as a valuable tool in research laboratories for studying stereochemistry and developing chiral catalysts. Its high enantioselectivity makes it a preferred choice for resolving complex organic molecules.
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