131029-14-6

Basic information

• Product Name: Acetic acid (S)-2-hydroxy-2-(4-methoxy-phenyl)-ethyl ester
• Synonyms: Acetic acid (S)-2-hydroxy-2-(4-methoxy-phenyl)-ethyl ester
• CAS NO: 131029-14-6
• Molecular Weight: 210.23
• Mol File: 131029-14-6.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Acetic acid (S)-2-hydroxy-2-(4-methoxy-phenyl)-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Acetic acid (S)-2-hydroxy-2-(4-methoxy-phenyl)-ethyl ester(131029-14-6)
• EPA Substance Registry System: Acetic acid (S)-2-hydroxy-2-(4-methoxy-phenyl)-ethyl ester(131029-14-6)

Safety Data

• Hazardous Substances Data: 131029-14-6(Hazardous Substances Data)

Upstream product

• 4136-21-4 p-methoxybenzoylmethanol 
• 637-69-4 4-Methoxystyrene 
• 64-19-7 acetic acid 
• 141-78-6 ethyl acetate 
• 58518-78-8 p-methoxyphenacyl acetate 
• 108-05-4 vinyl acetate 
• 32345-64-5 1-(4-methoxyphenyl) ethane-1,2-diol 
• 108-24-7 acetic anhydride 
• 13603-63-9 (R)-1-(4-methoxyphenyl)ethane-1,2-diol 
• 79-21-0 peracetic acid 
• 2196-99-8 2-chloro-1-(4-methoxyphenyl)ethanone 

Downstream Products

• 86659-43-0 1-(4-methoxyphenyl)ethane-1,2-diyl diacetate 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 90-05-1 2-methoxy-phenol 
• 58518-78-8 p-methoxyphenacyl acetate 
• 32345-64-5 1-(4-methoxyphenyl) ethane-1,2-diol 

Relevant articles and documents

Visible light induced redox neutral fragmentation of 1,2-diol derivatives

A homogeneous, redox-neutral photo fragmentation of diol derivatives was developed. Under photo/hydrogen atom transfer (HAT) dual catalysis, diol derivatives such as lignin model compounds and diol monoesters undergo selective β C(sp3)-O bond cleavage to afford ketones, phenols and acids effectively.

CuI/l-proline-catalyzed selective one-step mono-acylation of styrenes and stilbenes

Vicinal di-oxygenation of styrene-type olefins was achieved with cheaper, less toxic CuI in the presence of l-proline as ligand and NaIO4 as the oxidant. This approach provides a straightforward and efficient access to mono-acylated diols from both styrene and stilbene derivatives with good to excellent yields and diastereoselectivity.

Chemoenzymatic synthesis of enantiomerically pure 1,2-diols employing immobilized lipase in the ionic liquid [bmim]PF6

Significantly enhanced enantioselectivity in the enzymatic kinetic resolution of 1,2-diols employing immobilized lipase from Pseudomonas cepacia (PS-C, 'Amano') results from the use of the ionic liquid [bmim]PF6 as reaction medium.