89497-03-0

Basic information

• Product Name: 2-Methyl-3-((R)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-succinic acid dimethyl ester
• CAS NO: 89497-03-0
• Molecular Weight: 392.329
• Mol File: 89497-03-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Methyl-3-((R)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-succinic acid dimethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Methyl-3-((R)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-succinic acid dimethyl ester(89497-03-0)
• EPA Substance Registry System: 2-Methyl-3-((R)-3,3,3-trifluoro-2-methoxy-2-phenyl-propionyloxy)-succinic acid dimethyl ester(89497-03-0)

Safety Data

• Hazardous Substances Data: 89497-03-0(Hazardous Substances Data)

Upstream product

• 85199-58-2 (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1S,2S)-1-furan-2-yl-2-methoxycarbonyl-propyl ester 
• 85199-58-2 (S)-3,3,3-Trifluoro-2-methoxy-2-phenyl-propionic acid (1S,2R)-1-furan-2-yl-2-methoxycarbonyl-propyl ester 
• 608-41-3 erythro-2-hydroxy-3-methylbutane-1,4-dioic acid 
• 63921-06-2 3-methyl-2-oxo-butane-1,4-dioic acid dimethyl ester 
• 91487-35-3 (2S,3R)-2-Acetoxy-3-methyl-succinic acid dimethyl ester 
• 91487-28-4 (2R,3R)-3-Acetoxy-3-furan-2-yl-2-methyl-propionic acid methyl ester 
• 85199-59-3 methyl (2R,3S)-3-(furan-2-yl)-3-hydroxy-2-methylpropanoate 
• 85199-60-6 (R-(R^*,R^*))-β-hydroxy-α-methyl-2-furanpropanoate 
• 39637-99-5 (S)-(+)-2-methoxy-2-trifluoromethyl-2-phenylacetyl chloride 
• 85199-55-9 methyl 3-(furan-2-yl)-2-methyl-3-oxopropanoate 
• 186581-53-3 diazomethane 
• 91487-33-1 dimethyl (2R,3S)-2-O-acetyl-3-methylmalate 
• 85199-57-1 (2S,3S)-methyl 3-(furan-2-yl)-3-hydroxy-2-methylpropanoate 
• 91487-27-3 3-Furan-2-yl-3-hydroxy-2-methyl-propionic acid methyl ester 

Relevant articles and documents

The use of microorganisms in organic synthesis. III. Microbiological asymmetric reduction of methyl 3-(-2-furyl)-2-methyl-3-oxopropionate

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SYNTHESIS OF FUNCTIONALIZED CHIRAL SYNTHONS VIA MICROBIOLOGICAL REDUCTION

Four functionalized chiral synthons 1-4 having high optical purity were prepared by microbiological asymmetric reduction.