267228-34-2

Basic information

• Product Name: (S)-2-acetyloxy-3-(4-benzyloxyphenyl)propionic acid
• Synonyms: (S)-2-acetyloxy-3-(4-benzyloxyphenyl)propionic acid
• CAS NO: 267228-34-2
• Molecular Weight: 314.338
• Mol File: 267228-34-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: (S)-2-acetyloxy-3-(4-benzyloxyphenyl)propionic acid(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2-acetyloxy-3-(4-benzyloxyphenyl)propionic acid(267228-34-2)
• EPA Substance Registry System: (S)-2-acetyloxy-3-(4-benzyloxyphenyl)propionic acid(267228-34-2)

Safety Data

• Hazardous Substances Data: 267228-34-2(Hazardous Substances Data)

Upstream product

• 16652-64-5 O-benzyl-S-tyrosine 
• 127-09-3 sodium acetate 
• 60-18-4 L-tyrosine 
• 64-19-7 acetic acid 
• 65733-15-5 (R)-2-amino-3-(4-(benzyloxy)phenyl)propanoic acid 

Downstream Products

• 444911-11-9 C₄₉H₆₆N₆O₁₀ 
• 23508-35-2 (S)-2-hydroxy-3-(4-hydroxy-phenyl)-propionic acid 
• 501368-60-1 (2R,3aR,6R,7aR)-6-Acetoxy-1-{(R)-2-[(S)-2-acetoxy-3-(4-benzyloxy-phenyl)-propionylamino]-4-methyl-pentanoyl}-octahydro-indole-2-carboxylic acid methyl ester 
• 501368-66-7 AcO-L-Hpla(Bn)-D-Leu-3a,7a-diepi-L-Choi(OAc)-OMe 

Relevant articles and documents

Stereoselective Modification of N-(α-Hydroxyacyl)-glycinesters via Palladium-Catalyzed Allylic Alkylation

N-(α-Hydroxyacyl)-glycinesters can be used as excellent nucleophiles in Pd-catalyzed allylic alkylation. The method allows for the stereoselective introduction of a wide range of side chains, including highly functionalized ones. Both diastereomers can be accessed through variation of the reaction conditions. Furthermore, the use of stannylated carbonates introduces vinylstannane motifs, which are eligible for subsequent C-C coupling reactions.

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