592506-96-2

Upstream product

• 592506-95-1 (S)-4-((R)-1-Benzyloxy-octyl)-3-hexanoyl-1-(4-nitro-benzenesulfonyl)-imidazolidin-2-one 
• 592506-94-0 (S)-5-((R)-1-Benzyloxy-octyl)-1-hexanoyl-imidazolidin-2-one 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 
• 142-61-0 Hexanoyl chloride 

Downstream Products

• 592506-97-3 Hexanoic acid ((1S,2R)-1-aminomethyl-2-benzyloxy-nonyl)-amide 
• 592506-99-5 C₂₈H₅₂N₃O₅P 
• 592506-98-4 ((2S,3R)-3-Benzyloxy-2-hexanoylamino-decyl)-phosphoramidic acid 2-bromo-ethyl ester methyl ester 

Relevant academic research and scientific papers

Synthesis of a nitrogen analogue of sphingomyelin as a sphingomyelinase inhibitor

Matrix presented Sphingomyelin nitrogen analogue 1 was designed and synthesized as a sphingomyelinase inhibitor. The synthesis was established by continuous Hofmann rearrangement and Crutius rearrangement as key steps in constructing the 3-hydroxy-1,2-dia