869093-44-7

Basic information

• Product Name: (S)-2,5-dimethoxyphenyl 2-hydroxy-3-(4-pivaloyloxyphenyl)propanoate
• Synonyms: (S)-2,5-dimethoxyphenyl 2-hydroxy-3-(4-pivaloyloxyphenyl)propanoate
• CAS NO: 869093-44-7
• Molecular Weight: 402.444
• Mol File: 869093-44-7.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-2,5-dimethoxyphenyl 2-hydroxy-3-(4-pivaloyloxyphenyl)propanoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-2,5-dimethoxyphenyl 2-hydroxy-3-(4-pivaloyloxyphenyl)propanoate(869093-44-7)
• EPA Substance Registry System: (S)-2,5-dimethoxyphenyl 2-hydroxy-3-(4-pivaloyloxyphenyl)propanoate(869093-44-7)

Safety Data

• Hazardous Substances Data: 869093-44-7(Hazardous Substances Data)

Upstream product

• 58305-26-3 p-(bromomethyl)phenyl pivalate 
• 59012-91-8 2,2-dimethyl-propionic acid 4-hydroxymethyl-phenyl ester 
• 3282-30-2 pivaloyl chloride 
• 623-05-2 (4-hydroxyphenyl)methanol 
• 869093-41-4 (S)-4-(2-(benzhydryloxy)-3-(2,5-dimethoxyphenyl)-3-oxopropyl)phenyl pivalate 
• 869093-43-6 (S)-4-(3-(2,5-dimethoxyphenyl)-2-hydroxy-3-oxopropyl)phenyl pivalate 

Downstream Products

• 915396-55-3 (S)-2-hydroxy-3-(4-hydroxyphenyl)-N-methoxy-N-methylpropanamide 
• 915396-57-5 (S)-4-(3-(methoxy(methyl)amino)-3-oxo-2-(triethylsilyloxy)propyl)phenyl pivalate 
• 915396-58-6 (S)-4-(3-oxo-4-phenyl-2-(triethylsilyloxy)butyl)phenyl pivalate 
• 222834-30-2 ragaglitazar 
• 222834-42-6 (S)-methyl 3-(4-(2-(10H-phenoxazin-10-yl)ethoxy)phenyl)-2-ethoxypropanoate 
• 325793-74-6 (S)-methyl 2-ethoxy-3-(4-hydroxyphenyl)propanoate 
• 915396-60-0 (S)-4-(2-hydroxy-3-(methoxy(methyl)amino)-3-oxopropyl)phenyl pivalate 
• 869093-45-8 (S)-3-[4-(2,2-Dimethyl-propionyloxy)-phenyl]-2-ethoxy-propionic acid 2,5-dimethoxy-phenyl ester 

Relevant articles and documents

Total synthesis of the hydroxyketone kurasoin A using asymmetric phase-transfer alkylation

The total synthesis of the farnesyltransferase inhibitor kurasoin A has been achieved using a novel asymmetric phase-transfer-catalyzed glycolate alkylation reaction. 2,5-Dimethoxyacetophenone 7 with cinchonidinium catalyst 9 (10 mol %) and hydroxide base