247592-53-6

Basic information

• Product Name: 1,1-dimethylethyl 6-cyanomethyl-2,2-dimethyl-1,3-dioxane-4-acetate
• CAS NO: 247592-53-6
• Molecular Weight: 269.341
• Mol File: 247592-53-6.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1,1-dimethylethyl 6-cyanomethyl-2,2-dimethyl-1,3-dioxane-4-acetate(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-dimethylethyl 6-cyanomethyl-2,2-dimethyl-1,3-dioxane-4-acetate(247592-53-6)
• EPA Substance Registry System: 1,1-dimethylethyl 6-cyanomethyl-2,2-dimethyl-1,3-dioxane-4-acetate(247592-53-6)

Safety Data

• Hazardous Substances Data: 247592-53-6(Hazardous Substances Data)

Upstream product

• 773837-37-9 sodium cyanide 
• 312745-90-7 tert-butyl (5S)-6-cyano-5-hydroxy-3-oxohexanoate 
• 125988-01-4 tert-butyl (5R)-6-cyano-5-hydroxy-3-carbonylhexanoate 
• 144-55-8 sodium hydrogencarbonate 
• 125971-93-9 (3R,5R)-tert-butyl-6-cyano-3,5-dihydroxyhexanoate 

Relevant articles and documents

Preparation method of 3,5,6-substitued caproate derivative

The invention discloses a preparation method of a 3,5,6-substitued caproate derivative which is represented as the general formula (I), wherein the method is prepared with lactone as a raw material and an iodinated substance as an intermediate. The method is low in raw material cost, employs simple reactions, is stable and is high in yield, is easy to control and is suitable for large-scale industrial production.

Process for the synthesis of 1,3-diols

An improved process for the preparation of cis-1,3-diols is described where a beta hydroxy ketone is treated with a trialkylborane or dialkylalkoxyborane or a mixture of a trialkylborane and a dialkylalkoxyborane followed by recovery and reuse of the alkylborane species to convert additional beta hydroxy ketone to the cis-1,3-diol.

Process for the synthesis of (5R)-1,1-dimethylethyl-6-cyano-5-hydroxy-3-oxo-hexanoate

An improved process for the preparation of (5R)-1,1-dimethylethyl-6-cyano-5-hydroxy-3-oxo-hexanoate is described where a halo hydroxyester or other activated dihydroxyester is converted in two steps to the desired product.