170238-75-2

Basic information

• Product Name: (R)-(+)-2,2,4-Trimethyl-4-<2-(benzyloxy)ethyl>-1,3-dioxolane
• Synonyms: (R)-(+)-2,2,4-Trimethyl-4-<2-(benzyloxy)ethyl>-1,3-dioxolane
• CAS NO: 170238-75-2
• Molecular Weight: 250.338
• Mol File: 170238-75-2.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (R)-(+)-2,2,4-Trimethyl-4-<2-(benzyloxy)ethyl>-1,3-dioxolane(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-(+)-2,2,4-Trimethyl-4-<2-(benzyloxy)ethyl>-1,3-dioxolane(170238-75-2)
• EPA Substance Registry System: (R)-(+)-2,2,4-Trimethyl-4-<2-(benzyloxy)ethyl>-1,3-dioxolane(170238-75-2)

Safety Data

• Hazardous Substances Data: 170238-75-2(Hazardous Substances Data)

Upstream product

• 100-39-0 benzyl bromide 
• 77-76-9 2,2-dimethoxy-propane 
• 1679-47-6 3-methyltetrahydro-2-furanone 
• 93206-60-1 (S)-4-methyl-4-(trichloromethyl)-2-oxetanone 
• 81426-68-8 (R)-dimethyl 2-hydroxy-2-methylsuccinate 
• 81426-65-5 (R)-(+)-2-Methylbutane-1,2,4-triol 
• 6236-10-8 (R)-(-)-citramalic acid 
• 79243-90-6 (R)-4-(2'-hydroxyaethyl)-2,2,4-trimethyl-1,3-dioxolan 

Downstream Products

• 252651-57-3 (R)-2-methyl-2-[2'-(phenylmethoxy)ethyl]oxirane 
• 300661-16-9 (S)-4-(2',5'-dimethoxyphenyl)-3-hydroxy-3-methylbutanal 
• 300661-19-2 (S)-4-(2',5'-dimethoxyphenyl)-3-methylbutane-1,3-diol 
• 300661-17-0 (R)-2-hydroxy-2-methyl-4-(phenylmethoxy)butyl methanesulfonate 
• 300661-18-1 (S)-4-benzyloxy-1-(2',5'-dimethoxyphenyl)-2-methylbutan-2-ol 
• 170238-76-3 (R)-2-methyl-4-(phenylmethoxy)butane-1,2-diol 

Relevant articles and documents

Pigments of Fungi. LIX - Synthesis of (1S,3S)- and (1R,3R)-austrocortilutein and (1S,3S)-austrocortirubin from citramalic acid

The naturally occurring tetrahydroanthraquinone (1S,3S)-austrocortilutein (1) is synthesized for the first time in enantiomerically pure form by Diels-Alder cycloaddition between the functionalized butadiene derivative (8) and the chiral 1,3-dihydroxy-1,2,3,4-tetrahydro-5,8-naphthoquinone (9), the latter being derived from (R)-citramalic acid (3). The natural products (1S,3S)-austrocortirubin (2) and (1R,3R)-austrocortilutein (5) were also prepared for the first time by using the same strategy. CSIRO 2000.