1030350-22-1

Basic information

• Product Name: (2E)-5-(2-benzyloxy-phenyl)-pent-2-enoic acid ethyl ester
• Synonyms: (2E)-5-(2-benzyloxy-phenyl)-pent-2-enoic acid ethyl ester
• CAS NO: 1030350-22-1
• Molecular Weight: 310.393
• Mol File: 1030350-22-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2E)-5-(2-benzyloxy-phenyl)-pent-2-enoic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (2E)-5-(2-benzyloxy-phenyl)-pent-2-enoic acid ethyl ester(1030350-22-1)
• EPA Substance Registry System: (2E)-5-(2-benzyloxy-phenyl)-pent-2-enoic acid ethyl ester(1030350-22-1)

Safety Data

• Hazardous Substances Data: 1030350-22-1(Hazardous Substances Data)

Upstream product

• 75677-03-1 3-(2-benzyloxy-phenyl)-propionaldehyde 
• 1099-45-2 ethyl (triphenylphosphoranylidene)acetate 

Downstream Products

• 1030350-24-3 (2R,3S)-5-(2-benzyloxy-phenyl)-2,3-dihydroxy-pentanoic acid ethyl ester 
• 1177405-69-4 (E)-5[2-(benzyloxy)-5-methoxyphenyl]pent-2-en-1-ol 
• 1132981-78-2 (2S,3R)-ethyl 5-(2-(benzyloxy)phenyl)-2,3-dihydroxypentanoate 

Relevant articles and documents

β-Hydroxy-α-tosyloxy esters as chiral building blocks for the enantioselective synthesis of benzo-annulated oxa-heterocycles: scope and limitations

The enantioselective synthesis of benzo-annulated oxa-heterocycles 2,3-dihydrobenzofuran and 1-benzopyran derivatives is described using β-hydroxy-α-tosyloxy esters as chiral building blocks, which are easily accessible through the regioselective α-tosyla

Application of phenolate ion mediated intramolecular epoxide ring opening in the enantioselective synthesis of functionalized 2,3-dihydrobenzofurans and 1-benzopyrans

The enantioselective synthesis of 2-isopropenyl-2,3-dihydrobenzofurans, 4-(2,3-dihydrobenzofuran-2-yl)-2-methylbut-3-en-2-ols, 2-hydroxymethyl chromans, and 4-chroman-2-yl-2-methylbut-3-en-2-ols has been achieved using Sharpless asymmetric epoxidation-der