217495-57-3

Basic information

• Product Name: [2R]-dibenzylamino-3-(tetrahydropyran-2-yloxy)propionic acid methyl ester
• Synonyms: [2R]-dibenzylamino-3-(tetrahydropyran-2-yloxy)propionic acid methyl ester
• CAS NO: 217495-57-3
• Molecular Weight: 383.488
• Mol File: 217495-57-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: [2R]-dibenzylamino-3-(tetrahydropyran-2-yloxy)propionic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: [2R]-dibenzylamino-3-(tetrahydropyran-2-yloxy)propionic acid methyl ester(217495-57-3)
• EPA Substance Registry System: [2R]-dibenzylamino-3-(tetrahydropyran-2-yloxy)propionic acid methyl ester(217495-57-3)

Safety Data

• Hazardous Substances Data: 217495-57-3(Hazardous Substances Data)

Upstream product

• 110-87-2 3,4-dihydro-2H-pyran 
• 202478-34-0 (R)-methyl 2-(dibenzylamino)-3-hydroxypropanoate 
• 100-39-0 benzyl bromide 

Downstream Products

• 214596-89-1 {[1R,2S]-2-[4-(1-hydroxy-2-nitroethyl)phenoxy]-3-methyl-1-(tetrahydropyran-2-yloxymethyl)butyl}carbamic acid tert-butyl ester 
• 214596-93-7 {[1R,2S]-2-[4-(2-amino-1-hydroxyethyl)-phenoxy]-3-methyl-1-(tetrahydropyran-2-yloxymethyl)butyl}carbamic acid tert-butyl ester 
• 214596-88-0 [[1R,2S]-2-(4-cyanophenoxy)-3-methyl-1-(tetrahydropyran-2-yloxymethyl)butyl]carbamic acid tert-butyl ester 
• 214596-92-6 [[1R,2S]-2-(4-formylphenoxy)-3-methyl-1-(tetrahydropyran-2-yloxymethyl)butyl]carbamic acid tert-butyl ester 
• 214596-91-5 4-[[1S,2R]-2-amino-1-isopropyl-3-(tetrahydropyran-2-yloxy)propoxy]benzonitrile 
• 214596-90-4 ([1R,2S]-2-{4-[2-(2S-benzyloxycarbonylamino-4-methylpentanoylamino)-1-hydroxyethyl]-phenoxy}-3-methyl-1-(tetrahydropyran-2-yloxymethyl)butyl)carbamic acid tert-butyl ester 
• 217495-58-4 [2S]-dibenzylamino-3-(tetrahydropyran-2-yloxy)propan-1-ol 

Relevant articles and documents

Total synthesis of the cyclopeptide alkaloid sanjoinine G1 and its C-11 epimer

The naturally occurring cyclopeptide alkaloid sanjoinine G1 and its C- 11 epimer were synthesized in 18 steps from D-serine. The key steps in the synthesis were the formation of the alkylaryl ether linkage via an S(N)Ar reaction with 4-fluorobenzonitrile