51513-41-8

Usage

Uses

Used in Organic Synthesis:
2,7-Dimethyloctane-3,6-dione is used as a building block in organic synthesis for the preparation of various other chemicals. Its unique structure and reactivity make it a valuable component in the creation of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,7-Dimethyloctane-3,6-dione is used as an intermediate in the synthesis of pharmaceutical compounds. Its antioxidant properties may also contribute to the development of new drugs with potential health benefits.
Used in Food Additives Industry:
2,7-Dimethyloctane-3,6-dione is used as a food additive due to its antioxidant properties. It helps to extend the shelf life of food products by preventing oxidation and spoilage, ensuring freshness and quality.
Safety Precautions:
It is important to handle 2,7-Dimethyloctane-3,6-dione with care, as it may cause irritation to the skin, eyes, and respiratory system if not properly managed. Appropriate safety measures, such as wearing protective gear and working in a well-ventilated area, should be taken to minimize potential risks.

Upstream product

• 1068-55-9 isopropylmagnesium chloride 
• 123-25-1 succinic acid diethyl ester 
• 563-80-4 3-methyl-butan-2-one 
• 1518-06-5 1,3-dibromo-3-methyl-2-butanone 
• 31206-61-8 2,7-dimethyl-3,6-octanediol 
• 7664-93-9 sulfuric acid 
• 64-19-7 acetic acid 
• 71-43-2 benzene 
• 85796-26-5 acide (isopropyl-2 dioxolanne-1,3 yl-2)-2 acetique 
• 85796-22-1 dioxolanne du methyl-4 oxo-3 pentanoate de methyle 
• 157872-91-8 2-Isobutyryl-5-methyl-4-oxo-hexanoic acid methyl ester 
• 85796-32-3 bis (isopropyl-2 dioxolanne-1,3 yl-2)-1,2 ethane 
• 69278-36-0 3-bromo-3-methyl-2-trimethylsiloxy-1-butene 
• 7694-48-6 (1-isopropyl-vinyl)-dimethyl-amine 

Downstream Products

• 55959-72-3 2-(2,5-Di-isopropyl-pyrrol-1-yl)amino-4,5-dihydro-1H-imidazole 
• 31206-61-8 2,7-dimethyl-3,6-octanediol 
• 75924-54-8 (S*,R*)-2,7-dimethyl-3,6-octanediol 
• 31206-61-8 (S*,S*)-2,7-dimethyl-3,6-octanediol 
• 1432480-22-2 1,1'-(2-methoxy-1,3-phenylene)bis(2,5-diisopropylpyrrolyl) 
• 1232366-57-2 DPPBr 

Relevant academic research and scientific papers

Diacylation of activated olefins promoted by electrochemically generated NO3·

It has been found in this study that an acyl radical is formed by the reaction of an aldehyde with a radical NO3· generated by the anodic oxidation of NO3- and the reaction of this acyl radical with activated olefins lead to the formation of a diacylated compound.

3′,3′-N-bis-desmethyl-3′-N-cycloalkyl erythromycin derivatives as LHRH antagonists

Disclosed are 3′,3′-N-bis-desmethyl-3′-N-cycloalkyl-6-O-methyl-11-deoxy-11,12-cyclic carbamate erythromycin A derivatives which are antagonists of lutenizing hormone-releasing hormone (LHRH). Also disclosed are pharmaceutical compositions comprising the compounds, to methods of using the compounds and to the process of making the same.

Preparation and Reactivities of (η3-1- and 2-Trimethylsiloxyallyl)Fe(CO2)NO Complexes. Intermediates Functioning as Equivalents of β- and α-Acyl Carbocations and Acyl Carbanions

(η3-1- and 2-Trimethylsiloxyallyl)Fe(CO)2NO complexes were prepared by the reaction of the corresponding siloxyallylic halides with Bu4N.These complexes reacted with both of carbon nucleophiles and carbon electrophiles preferentially at the less hindered sites of the allylic ligands.In these reactions, (η3-1-trimethylsiloxyallyl)Fe(CO)2NO complexes served as synthetically equivalent synthons for both of β-acyl carbocations and β-acyl carbanions and (η3-2-trimethylsiloxyallyl)Fe(CO)2NO complexes as both of α-acyl carbocations and α-acyl carbanions.The stereochemical courses of the reactions are described.

Preparation et oxydation anodique d'acides β-cetaliques. Application a la synthese de γ-bisdioxolannes symetriques et des γ-dicetones derivees.

Anoxic oxidation of carboxylic acids with β-dioxolane substituents leads to good yields of symmetrical γ-bisdioxolanes.Hydrolysis of these compounds easily provides the corresponding γ-diketones.The synthesis of the starting acids is described.

Oxydation anodique de β-cetocarboxylates en milieu aqueux ou hydroorganique. Application a la synthese de γ-dicetones, de cetones ethyleniques et de cetoamides

A systematic study of the anodic oxidation of β-ketocarboxylate anions in aqueous or hydroorganic solvents allows to distinguish the factors directing this reaction.Thus, it is possible by the appropriate choice of reaction medium and structure of the starting ion to synthesize products such as γ diketones, ethylenic ketones and ketoamides.