112378-35-5

Basic information

• Product Name: 5-(cyclohexanecarbonyl)-2,2-dimethyl-1,3-dioxane-4,6-dione
• Synonyms: 5-(cyclohexanecarbonyl)-2,2-dimethyl-1,3-dioxane-4,6-dione
• CAS NO: 112378-35-5
• Molecular Weight: 254.283
• Mol File: 112378-35-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 5-(cyclohexanecarbonyl)-2,2-dimethyl-1,3-dioxane-4,6-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(cyclohexanecarbonyl)-2,2-dimethyl-1,3-dioxane-4,6-dione(112378-35-5)
• EPA Substance Registry System: 5-(cyclohexanecarbonyl)-2,2-dimethyl-1,3-dioxane-4,6-dione(112378-35-5)

Safety Data

• Hazardous Substances Data: 112378-35-5(Hazardous Substances Data)

Upstream product

• 2033-24-1 cycl-isopropylidene malonate 
• 2719-27-9 cyclohexanylcarbonyl chloride 
• 98-89-5 Cyclohexanecarboxylic acid 

Downstream Products

• 112378-46-8 3-tert-Butyl-5-cyclohexanecarbonyl-2-phenyl-[1,3]oxazinane-4,6-dione 
• 112632-05-0 3-tert-Butyl-6-cyclohexyl-4-oxo-2-phenyl-3,4-dihydro-2H-[1,3]oxazine-5-carboxylic acid 
• 112378-60-6 6-Cyclohexyl-2,3-diphenyl-2,3-dihydro-[1,3]oxazin-4-one 
• 1351575-89-7 methyl 6-cyclohexyl-2-oxo-4-(trifluoromethyl)-2H-pyran-5-carboxylate 
• 1351575-90-0 6-cyclohexyl-4-(trifluoromethyl)-2H-pyran-2-one 
• 1351572-60-5 6-cyclohexyl-1-hydroxy-4-(trifluoromethyl)pyridin-2(1H)-one 

Relevant articles and documents

Preparation method of tenuazonic Acid and derivative thereof

The invention provides a preparation method of tenuazonic Acid and a derivative thereof. The synthesis route comprises the following steps: reacting malonic acid cycloisopropylidene ester with acyl chloride, then reacting with amino acid methyl ester hydr

Amic acid derivative as well as preparation method and application thereof

The invention provides an amine acid derivative as well as a preparation method and application thereof. The amine acid derivative has the structure as follows. Herein, R is selected from methyl, methoxy and the like. R1 Selected from C1 - C4 a

1,3-Oxazines and Related Compounds. XIII. Reaction of Acyl Meldrum's Acids with Schiff Bases Giving 2,3-Disubstituted 5-Acyl-3,4,5,6-tetrahydro-2H-1,3-oxazine-4,6-diones and 2,3,6-Trisubstituted 2,3-Dihydro-1,3-oxazin-4-ones

The reaction of Schiff bases (2) with various acyl Meldrum's acids (1) were investigated.Refluxing of 1 and 2 in benzene caused an exchange reaction of the acetone moiety of 1 with the Schiff base moiety through the intermediate acylketenes 11 formed in s