![(1S)-1-[[4-[2-benzyloxy-5-[[(1R)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phe…](/_next/image/?url=https%3A%2Fstatic.cymitquimica.com%2Fcas-image%2Fthumb-webp%2F385264-1s-1-4-2-benzyloxy-5-1r-67-dimethoxy-2-methyl-34-dihydro-1h-isoquinolin-1-yl-methyl-phenoxy-phenyl-methyl-67-dimethoxy-2-methyl-34-dihydro-1h-isoquinoline.webp&w=3840&q=75)
CAS 2748-99-4: (1S)-1-[[4-[2-benzyloxy-5-[[(1R)-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinolin-1-yl]methyl]phenoxy]phenyl]methyl]-6,7-dimethoxy-2-methyl-3,4-dihydro-1H-isoquinoline
Formula:C45H50N2O6
InChI:InChI=1/C45H50N2O6/c1-46-20-18-33-25-41(48-3)43(50-5)27-36(33)38(46)22-30-12-15-35(16-13-30)53-45-24-32(14-17-40(45)52-29-31-10-8-7-9-11-31)23-39-37-28-44(51-6)42(49-4)26-34(37)19-21-47(39)2/h7-17,24-28,38-39H,18-23,29H2,1-6H3/t38-,39+/m0/s1
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O-Benzyl-dauricidin
CAS:O-Benzyl-dauricidin is an intermediate in the synthesis of methiodide, chloride and diamide. It is a stereoisomeric compound which can be used to produce either the meso or racemic form. The meso form is more stable than the racemic form. O-Benzyl-dauricidin is produced by condensation and cyclization of ethylene oxide and methylamine. This process can also be carried out using methylene chloride instead of ethylene oxide.Formula:C45H50N2O6Purity:Min. 95%Molecular weight:714.89 g/mol