85963-71-9

Usage

Uses

Used in Chelating Applications:
3-(carboxymethyl)-3-methylpentanedioic acid is used as a chelating agent for its ability to bind metal ions, which is beneficial in various industrial processes.
Used in the Food Industry:
3-(carboxymethyl)-3-methylpentanedioic acid is used as a preservative and flavoring agent in the food industry, where its chelating properties help to extend the shelf life and enhance the taste of food products.
Used in Agriculture:
3-(carboxymethyl)-3-methylpentanedioic acid is used in agriculture for its potential antifungal properties, which can help protect crops from fungal infections and improve yield.
Used in Pharmaceutical Applications:
3-(carboxymethyl)-3-methylpentanedioic acid is used as a therapeutic agent for its ability to inhibit certain enzymatic processes, making it a potential treatment for metabolic disorders.

Upstream product

• 924-59-4 diethyl 3-methylpent-2-enedioate 
• 85963-72-0 4-Methyl-2,6-dioxo-4-piperidinessigsaeure 
• 85963-69-5 α-Cyanethan-1,1,1-triessigsaeure-triethylester 

Downstream Products

• 861321-71-3 3-(ethoxycarbonyl-bromo-methyl)-2,4-dibromo-3-methyl-glutaric acid diethyl ester 
• 85963-61-7 1,5-dihydroxy-3-(2-hydroxyethyl)-3-methylpentane 
• 85963-67-3 1,1,1-Ethantriacetylchlorid 
• 883866-55-5 (4-methyl-2,6-dioxo-tetrahydro-pyran-4-yl)-acetyl chloride 
• 503416-46-4 3-(methoxycarbonyl)methyl-3-methyl-pentane-1,5-dicarboxylic acid-dimethylester 
• 85963-53-7 7-Methyl-7-(2-oxohexyl)-5,9-tridecandion 
• 85963-52-6 4-Methyl-4-(2-oxopropyl)-2,6-heptandion 
• 85963-57-1 1,3,5,7-Tetramethyl-2,4-dioxa-9-azatricyclo<3.3.1.1^3,7>decane 
• 85963-56-0 3,5,7-Trimethyl-2,4-dioxatricyclo<3.3.1.1^3,7>decan-1-ol 
• 85963-62-8 1,5-Dibrom-3-(2-bromethyl)-3-methylpentan 

Relevant academic research and scientific papers

Methanetriacetic and methylmethanetriacetic acids, their precursors and derivatives: NMR and X-ray diffraction studies

The NMR spectra and crystal structures of triacid 2b, triamide 4b and diastereomers 7, 8 were studied; the crystal structure of 2b is the first example of an H-bonded totally interlocked and percatenated homochiral structure.

2,4-Dioxa-, 2,4,9-Trioxa-, 2,4-Dioxa-9-aza-, 2-Oxa-4,9-diaza-, and 2,4,9-Triazaadamantanes

The reaction of the trihalides 7a, b with sodium cyanide in dimethylformamide afforded the cyclopropanedicarbonitrile 9 instead of of the tricarbonitrile 7c which had been designed as a precursor to 2,4,9-triazaadamantanes.Both the photolysis and thermolysis of the remarkably stable triazide 13c proceeded in an ill-defined way, producing unidentifiable products among which neither the triazaadamantane 6a nor hydrolysis products of the triimine 14 could be detected.The readily cyclizing triketone 3l was obtained from the reaction of the tricarbonyl chloride 3k with an excess of lithium dimethylcuprate followed by careful work-up.It proved to be the key to several novel heteroadamantanes: Thus, methoxide brought about an intramolecular aldol addition and cyclization of 3l to the 2,4-dioxaadamantane 15.An excess of liquid ammonia converted 3l into the 2,4-dioxa-9-azaadamantane 16a almost quantitatively.The same ring system (16b) was formed in the reaction of 3l with 12 mol of hydrazine hydrate.In contrast, the reaction of 3l with a very large excess of hydrazine hydrate afforded the 2-oxa-4,9-diazaadamantane 16c.Finally, 3l reacted with dry hydrazine in ethanol to yield the 2,4,9-triazaadamantane 16d.The structures of the new compounds were established by IR and NMR spectroscopy.Analysis of the complex 1H NMR multiplets of the methylene protons of 15 and 16a - c by LAOCOON III shows that they arise exclusively from W-couplings of 2 - 3 Hz and geminal couplings.