54814-41-4

Basic information

• Product Name: 3-(3,4-dimethoxy-phenyl)-2-hydroxy-propionic acid methyl ester
• CAS NO: 54814-41-4
• Molecular Weight: 240.256
• Mol File: 54814-41-4.mol
• Article Data: 19

Chemical Properties

• CAS DataBase Reference: 3-(3,4-dimethoxy-phenyl)-2-hydroxy-propionic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3,4-dimethoxy-phenyl)-2-hydroxy-propionic acid methyl ester(54814-41-4)
• EPA Substance Registry System: 3-(3,4-dimethoxy-phenyl)-2-hydroxy-propionic acid methyl ester(54814-41-4)

Safety Data

• Hazardous Substances Data: 54814-41-4(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 23028-17-3 danshensu 
• 188896-01-7 (Z)-3-(3,4-Dimethoxy-phenyl)-2-hydroxy-acrylic acid methyl ester 
• 54844-37-0 (R)-3-(3,4-dimethoxyphenyl)-2-hydroxypropanoic acid 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 75-16-1 methylmagnesium bromide 
• 690639-23-7 methyl 2-azido-3-(3',4'-dimethoxyphenyl)-propenoate 
• 108-05-4 vinyl acetate 
• 54814-41-4 (+/-)-(R)-methyl 3-(3,4-dimethoxyphenyl)-2-hydroxypropanoate 
• 312908-57-9 (2R,3S)-methyl 3-(3,4-dimethoxyphenyl)-2,3-dihydroxypropanoate 
• 130286-76-9 (1S,2R)-1-(3,4-Dimethoxy-phenyl)-6,7-dimethoxy-1,2-dihydro-naphthalene-2,3-dicarboxylic acid bis-[(R)-2-(3,4-dimethoxy-phenyl)-1-methoxycarbonyl-ethyl] ester 
• 119152-55-5 decamethylrabdosiin 
• 130396-77-9 anthocerotonic acid 
• 179188-11-5 (2S)-3-(3,4-dihydroxyphenyl)-2-{[(2E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy}propanoic acid 

Downstream Products

• 170801-79-3 (R)-(+)-N-(2,2-Dimethoxyethyl)-3-(3,4-dimethoxyphenyl)-2-hydroxypropionate 
• 55757-14-7 (2S,3S)-methyl 2-(3,4-dimethoxyphenyl)-4-((E)-3-(((R)-3-(3,4-dimethoxyphenyl)-1-methoxy-1-oxopropan-2-yl)oxy)-3-oxoprop-1-en-1-yl)-7-methoxy-2,3-dihydrobenzofuran-3-carboxylate 
• 1310802-43-7 (2R,3R)-methyl 2-(3,4-dimethoxyphenyl)-4-((E)-3-(((R)-3-(3,4-dimethoxyphenyl)-1-methoxy-1-oxopropan-2-yl)oxy)-3-oxoprop-1-en-1-yl)-7-methoxy-2,3-dihydrobenzofuran-3-carboxylate 
• 1400055-66-4 C₃₄H₃₄O₁₂ 
• 1400055-70-0 C₃₃H₃₂O₁₂ 
• 1283147-52-3 (R)-3-(3,4-dimethoxyphenyl)-1-methoxy-1-oxopropan-2-yl acrylate 
• 1403877-28-0 C₂₈H₂₈O₇ 
• 115841-16-2 (2R)-3-(3,4-dimethoxyphenyl)-1-methoxy-1-oxopropan-2-yl (2E)-3-[2-(3,4-dimethoxyphenyl)-7-methoxy-1-benzofuran-4-yl]prop-2-enoate 
• 1429320-11-5 methyl (2S)-3-(3,4-dimethoxyphenyl)-2-hydroxypropanoate 
• 54814-41-4 3-(3,4-dimethoxy-phenyl)-2-hydroxy-propionic acid methyl ester 
• 1429320-14-8 C₂₂H₃₀O₈S 
• 153381-08-9 Methyl (S)-(+)-3-(3,4 dimethoxyphenyl)-2-hydroxypropionate 
• 54814-41-4 (+/-)-(R)-methyl 3-(3,4-dimethoxyphenyl)-2-hydroxypropanoate 
• 35271-83-1 methyl 2-oxo 3-(3,4-dimethoxyphenyl) propanoate 

Relevant articles and documents

C28Terpenoids from Lamiaceous Plant Perovskia scrophulariifolia: Their Structures and Anti-neuroinflammatory Activity

Structurally unique C28 terpenoids, perovsfolins A (1) and B (2), were isolated from the aerial parts of an Uzbek medicinal plant, Perovskia scrophulariifolia (Lamiaceae). Their chemical structures including an unprecedented 6/8/6/6/6 pentacyclic carbon skeleton with a C6-C3 ester moiety were elucidated on the basis of spectroscopic analyses aided by density functional theory calculations as well as chemical evidence. Perovsfolin B (2) exhibited an anti-neuroinflammatory activity.

Stereoselective α-Hydroxylation of Amides Using Oppolzer's Sultam as Chiral Auxiliary

An Oppolzer's sultam-based highly stereoselective α-hydroxylation of amides was developed to deliver the desired products in good yield and excellent diastereoselectivity (>20/1). The generally crystalline products and the recyclability of the chiral auxiliary illustrate the practicability and scalability of the current approach.

Asymmetric transfer hydrogenation of α-azido acrylates

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