634893-08-6

Basic information

• Product Name: (2R,5R)-2-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-3,6-diethoxy-2-ethyl-5-isopropyl-2,5-dihydropyrazine
• Synonyms: (2R,5R)-2-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-3,6-diethoxy-2-ethyl-5-isopropyl-2,5-dihydropyrazine
• CAS NO: 634893-08-6
• Molecular Weight: 480.648
• Mol File: 634893-08-6.mol

Chemical Properties

• CAS DataBase Reference: (2R,5R)-2-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-3,6-diethoxy-2-ethyl-5-isopropyl-2,5-dihydropyrazine(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,5R)-2-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-3,6-diethoxy-2-ethyl-5-isopropyl-2,5-dihydropyrazine(634893-08-6)
• EPA Substance Registry System: (2R,5R)-2-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-3,6-diethoxy-2-ethyl-5-isopropyl-2,5-dihydropyrazine(634893-08-6)

Safety Data

• Hazardous Substances Data: 634893-08-6(Hazardous Substances Data)

Upstream product

• 110117-71-0 (2R)-3,6-diethoxy-2-isopropyl-2,5-dihydropyrazine 
• 94460-54-5 3-Methoxy-4-benzyloxy-phenethyliodid 
• 75-03-6 ethyl iodide 
• 634893-22-4 (2R,5R)-2-[2-(4-benzyloxy-3-methoxyphenyl)ethyl]-3,6-diethoxy-5-isopropyl-2,5-dihydropyrazine 

Downstream Products

• 634893-23-5 [1-ethyl-3-[3-methoxy-4-(4-phenyl-butoxy)-phenyl]-1-(3-oxo-1,5-dihydro-3λ⁵-benzo[e][1,3,2]dioxaphosphepin-3-yloxymethyl)-propyl]-carbamic acid tert-butyl ester 
• 634893-19-9 {1-ethyl-1-hydroxymethyl-3-[3-methoxy-4-(4-phenyl-butoxy)-phenyl]-propyl}-carbamic acid tert-butyl ester 
• 634893-16-6 [3-(4-benzyloxy-3-methoxy-phenyl)-1-ethyl-1-hydroxymethyl-propyl]-carbamic acid tert-butyl ester 
• 692755-15-0 [1-ethyl-3-(4-hydroxy-3-methoxy-phenyl)-1-hydroxymethyl-propyl]-carbamic acid tert-butyl ester 
• 634893-12-2 (R)-2-amino-4-(4-benzyloxy-3-methoxyphenyl)-2-ethylbutyric acid 

Relevant articles and documents

Synthesis of chiral analogues of FTY720 and its phosphate

Efficient and versatile protocols for the synthesis of chiral analogues of the novel immunomodulator FTY720 and its phosphate are described. These synthetic procedures allow for broad structural variation and deliver essential tools to further elucidate FTY720's novel mechanism of action.