55846-67-8

Usage

Appearance

White solid

Usage

Commonly used in organic synthesis and as a precursor for the production of other organic compounds

Chemical structure

Consists of two cyclohexyl groups attached to a 1,3-propanedione backbone

Applications

Wide range of applications in various industries, including pharmaceuticals, agrochemicals, and polymers

Reactivity

Versatile nature and reactivity make it a valuable building block for the synthesis of complex organic molecules

Safety

Important to handle with caution due to its potential flammability and toxicological properties

Upstream product

• 60718-45-8 1-cyclohexanecarbonyl-1H-imidazole 
• 98-89-5 Cyclohexanecarboxylic acid 
• 3289-28-9 ethyl cyclohexanecarboxylate 
• 823-76-7 Cyclohexyl methyl ketone 
• 64670-15-1 methyl 3-cyclohexyl-3-oxopropionate 
• 13898-94-7 3-cyclohexyl-3-oxopropanoic acid 
• 4630-82-4 methyl cyclohexylcarboxylate 

Downstream Products

• 250281-46-0 (+)-(R,R)-1,3-dicyclohexyl-1,3-propanediol 
• 223390-89-4 (S,S)-anti-1,3-dicyclohexyl-1,3-propanediol 
• 77486-19-2 (S,R)-1,3-dicyclohexyl-1,3-propanediol 

Relevant academic research and scientific papers

Synthesis method of multi-ring double-substituted 1,3 -propanedione compound (by machine translation)

The synthesis method comprises the following steps: under the protection of an inert gas, reacting the compound represented by the formula II with the compound of formula III under 1,3 - 1,3 - under the protection of inert gas to obtain the compound shown

NOVEL ORGANIC COMPOUND AND MATERIALS FOR ORGANIC ELECTROLUMINESCENT DEVICES COMPRISING THE SAME AND ORGANIC ELECTROLUMINESCENT DEVICES COMPRISING THE SAME

The present invention provides a novel organic compound represented by chemical formula 1, a material for an organic electroluminescent device including the organic compound, and an organic electroluminescent device. The present invention can improve color purity and device life.

Use of β-Ketocarboxylic Acids for Syntheses of 6-Substituted 4-Hydroxy-2-pyrones and Acyclic β-Diketones

β-Ketocarboxylic acids including β-ketoglutaric acid half-esters were cyclized by treating them with 1,1'-carbonyl-diimidazole to give 6-substituted 3-acyl-4-hydroxy-2-pyrones in good yields. 5-Aryl-3,5-dioxo-1-pentanoic acid and monomethyl malonate gave 6-aryl-4-hydroxy-2-pyrone and dimethyl β-ketoglutarate, respectively, on similar treatment.Anibin, one of the Aniba alkaloids, was synthesized from 5-(3-pyridyl)-4-hydroxy-2-pyrone.In addition, it was confirmed that reaction of magnesium β-ketocarboxylate with acylimidazolide gave the corresponding acyclic β-diketone in excellent yield.Keywords - β-ketocarboxilic acid; biogenetic-type synthesis; 4-hydroxy-2-pyrone; β-polyketide; β-ketoglutaric acid; dehydroacetic acid; anibin; Aniba alkaloid; 3-acyl-4-hydroxy-2-pyrone; β-diketone.

Preparation of antioxidants

This invention comprises an alkylation, reduction and transesterification process for the preparation of ester substituted phenols. The products are useful as antioxidants and may be prepared in high yields and with a high degree of purity.

3,5-Cycloalkyl pyrazolium salts as fungicides

There is provided a method for the control of plant pathogenic fungi with certain 3(5) or 3,5-cycloalkyl pyrazolium salts and to a method of protecting plants from fungal attack by applying to the foliage of said plants said pyrazolium salt in fungicidall