1041173-22-1

Basic information

• Product Name: methyl (3S)-4-[(4-methylphenyl)sulfonyl]morpholine-3-carboxylate
• Synonyms: methyl (3S)-4-[(4-methylphenyl)sulfonyl]morpholine-3-carboxylate
• CAS NO: 1041173-22-1
• Molecular Weight: 299.348
• Mol File: 1041173-22-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl (3S)-4-[(4-methylphenyl)sulfonyl]morpholine-3-carboxylate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (3S)-4-[(4-methylphenyl)sulfonyl]morpholine-3-carboxylate(1041173-22-1)
• EPA Substance Registry System: methyl (3S)-4-[(4-methylphenyl)sulfonyl]morpholine-3-carboxylate(1041173-22-1)

Safety Data

• Hazardous Substances Data: 1041173-22-1(Hazardous Substances Data)

Upstream product

• 98-59-9 p-toluenesulfonyl chloride 
• 17136-46-8 methyl (2S)-3-hydroxy-2-{[(4-methylphenyl)sulfonyl]amino}propanoate 
• 247129-85-7 (2-bromoethyl)(diphenyl)sulfonium trifluoromethanesulfonate 

Downstream Products

• 1041173-28-7 methyl (3S)-morpholine-3-carboxylate hydrobromide 

Relevant articles and documents

Synthesis of enantiopure 1,4-dioxanes, morpholines, and piperazines from the reaction of chiral 1,2-diols, amino alcohols, and diamines with vinyl selenones

The reactions of readily available vinyl selenones with enantiopure 1,2-diols, N-protected-1,2-aminoalcohols, and diamines gave substituted enantiopure 1,4-dioxanes, morpholines, and piperazines, respectively, in good to excellent yields. The same procedu

An annulation reaction for the synthesis of morpholines, thiomorpholines, and piperazines from β-heteroatom amino compounds and vinyl sulfonium salts

(Chemical Equation Presented) Heterocycling: Diphenyl vinyl sulfonium salt 1 acts first as an electrophile, then a base, and then again as an electrophile in this operationally simple, high yielding, one-pot synthesis of pharmacologically important morpholines, thiomorpholines, and piperazines. Compound 1 is an excellent synthon for the 1,2-ethane dication.