1443220-96-9

Upstream product

• 1374977-59-9 N-(4-fluoro-2-trifluoromethylphenyl)-2-(4-oxo-6-phenyl-3,4-dihydro-2H-1,5-benzothiazepin-5-yl)acetamide 
• 393-39-5 4-fluoro-2-(trifluoromethyl)aniline 
• 1443220-96-9 C₂₄H₁₈F₄N₂O₄S 
• 1374977-59-9 N-(4-fluoro-2-trifluoromethylphenyl)-2-(4-oxo-6-phenyl-3,4-dihydro-2H-1,5-benzothiazepin-5-yl)acetamide 
• 1443220-96-9 C₂₄H₁₈F₄N₂O₄S 
• 1443220-96-9 C₂₄H₁₈F₄N₂O₄S 
• 1374977-59-9 N-(4-fluoro-2-trifluoromethylphenyl)-2-(4-oxo-6-phenyl-3,4-dihydro-2H-1,5-benzothiazepin-5-yl)acetamide 

Downstream Products

• 1443220-96-9 C₂₄H₁₈F₄N₂O₄S 
• 1443220-96-9 C₂₄H₁₈F₄N₂O₄S 

Relevant academic research and scientific papers

Stereochemistry of 1,5-benzothiazepin-4-one S-oxide: Insight into the stereogenic elements at the sulfur atom and axis

Oxidation of 1,5-benzothiazepin-4-one (5-A) stereoselectively afforded the S-oxide 8I-A (aS,1S) in preference to the diastereomer 8II-A (aS,1R) affected by the remote stereogenic axis. All the enantiomers (8I-A/8I-B and 8II-A/8II-B) were separated and isolated, and the interconversion between 8I and 8II (equilibrium ratio ≈5:1) was unequivocally verified to be caused by the rotation around the axis.