252911-84-5

Basic information

• Product Name: methyl (4R)-benzyloxy-5-hydroxy-5-trans-2-pentenoate
• Synonyms: methyl (4R)-benzyloxy-5-hydroxy-5-trans-2-pentenoate
• CAS NO: 252911-84-5
• Molecular Weight: 236.268
• Mol File: 252911-84-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl (4R)-benzyloxy-5-hydroxy-5-trans-2-pentenoate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl (4R)-benzyloxy-5-hydroxy-5-trans-2-pentenoate(252911-84-5)
• EPA Substance Registry System: methyl (4R)-benzyloxy-5-hydroxy-5-trans-2-pentenoate(252911-84-5)

Safety Data

• Hazardous Substances Data: 252911-84-5(Hazardous Substances Data)

Upstream product

• 797037-71-9 (E)-(S)-5-Bromo-4-hydroxy-pent-2-enoic acid methyl ester 
• 252911-87-8 (E)-(R)-5-Bromo-4-hydroxy-pent-2-enoic acid methyl ester 
• 83541-54-2 methyl (4S)‐4,5‐dihydroxypent‐2‐enoate 
• 5927-18-4 trimethyl phosphonoacetate 
• 129492-58-6 (-)-2-O-benzyl-L-glyceraldehyde 
• 252911-92-5 methyl (4S)-4,5-epoxy-2(E)-pentenoate 
• 100-51-6 benzyl alcohol 

Downstream Products

• 252911-85-6 (E)-(R)-4-Benzyloxy-5-bromo-pent-2-enoic acid methyl ester 

Relevant articles and documents

Formal synthesis of (-)-anisomycin based on stereoselective nucleophilic substitution along with 1,2-aryl migration

The stereoselective conversion of (4R)-5-hydroxy-4-(4′-methoxyphenyl) -2(E)-pentenoate 4 into the (4S)-4-hydroxy-5-(4′-methoxyphenyl)-2(E)- pentenoate 5 using the AgNO3/MS 4 ?/MeNO2 system was accomplished along with complete inversi

Formal total synthesis of (-)-anisomycin based on the stereoselective nucleophilic substitution along with aryl migration

The stereoselective conversion of (4R)-5-hydroxy-4-(4'-methoxyphenyl)-2(E)-pentenoate 5 into the (4S)-4-hydroxy-5-(4'-methoxyphenyl)-2(E)-pentenoate 6 using an AgNO3/MS 4A/MeNO2 system was accomplished along with complete inversion a