CAS NO:100516-54-9 Benzyl (2R,3S)-(-)-6-oxo-2,3-diphenyl-4-morpholinecarboxylate
CAS NO:100516-54-9 NAME:Benzyl (2R,3S)-(-)-6-oxo-2,3-diphenyl-4-morpholinecarboxylate MF：C24H21NO4 MW：387.43 PURITY:97%+ COA:Available APPEARANCE:White solid
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Life Science Chemicals
Pharmaceutical Intermediates
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Product introduction
| PRODUCT NAME | Benzyl (2R,3S)-(-)-6-oxo-2,3-diphenyl-4-morpholinecarboxylate |
| CAS NO | 100516-54-9 |
| MP | 205-207 °C(lit.) |
| BP | 583.5±50.0 °C(Predicted) |
| DENSITY | 1.242±0.06 g/cm3(Predicted) |
| STORAGE | 2-8°C |
| DELIVERY | 2-3DAYS |
| PACKAGE | According client's request |
Description of CAS NO:100516-54-9 Benzyl (2R,3S)-(-)-6-oxo-2,3-diphenyl-4-morpholinecarboxylate
(2R,3S)-Benzyl 6-oxo-2,3-diphenylmorpholine-4-carboxylate, also known as B6ODPMC, is an important intermediate in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. B6ODPMC is a chiral compound, meaning it has two non-superimposable mirror images, and is composed of a benzyl group and a morpholine ring. B6ODPMC has been extensively studied for its potential applications in the synthesis of various compounds, and its mechanism of action and biochemical and physiological effects have been studied in detail.
(2R,3S)-Benzyl 6-oxo-2,3-diphenylmorpholine-4-carboxylate is a molecule with an enantioselective synthesis and a preparative method. It has been catalysed by chiral reagents such as chiral catalysts, chiral auxiliaries, and chiral ligands. This molecule can be synthesized in racemic form or in the form of its two enantiomers. The two enantiomers have different physical properties and biological activities. (2S,3S)-Benzyl 6-oxo-2,3-diphenylmorpholine-4-carboxylate is known to be an inhibitor of protein kinase C (PKC) that causes the release of intracellular calcium ions from cytoplasmic stores.
Applications of CAS NO:100516-54-9 Benzyl (2R,3S)-(-)-6-oxo-2,3-diphenyl-4-morpholinecarboxylate
1)Enantioselective Synthesis :
This compound has been utilized in the enantioselective synthesis of various amino acids and peptides.
2)Intermediate in CCR2 Antagonists Synthesis
3)Microbiological Production
4)Polymer Synthesis
5)Hyperbranched Polyamides
6)Nonclassical Antifolates Synthesis
7)Photocarboxylation in Drug Synthesis
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