92828-40-5

Usage

Uses

Used in Polymer Production:
1,1,2-Ethanetricarboxylic Acid, 2-(1,1-Dimethylethyl)1,1-Dimethyl Ester is used as a chemical intermediate for the synthesis of various polymer products. Its ester nature allows it to be incorporated into the production process, contributing to the formation of polymers with specific properties.
Used in Chemical Research:
Although not widely studied, 1,1,2-Ethanetricarboxylic Acid, 2-(1,1-Dimethylethyl)1,1-Dimethyl Ester may be used in chemical research to explore its potential applications and properties. Researchers may investigate its reactivity, stability, and interactions with other chemicals to better understand its potential uses and limitations.
Used in Industrial Applications:
1,1,2-Ethanetricarboxylic Acid, 2-(1,1-Dimethylethyl)1,1-Dimethyl Ester is used as a component in various industrial applications, where its chemical properties are leveraged to achieve specific outcomes. These applications may include the production of plastics, coatings, adhesives, or other materials that require the unique characteristics provided by this ester compound.
Used in Safety and Handling Protocols:
Due to the potential risks associated with handling 1,1,2-Ethanetricarboxylic Acid, 2-(1,1-Dimethylethyl)1,1-Dimethyl Ester, it is used as a reference in the development of safety and handling protocols. These protocols aim to minimize direct exposure and potential harm to individuals working with this chemical, ensuring a safer working environment.

Upstream product

• 5292-43-3 bromoacetic acid tert-butyl ester 
• 108-59-8 malonic acid dimethyl ester 

Downstream Products

• 128883-58-9 2-[(R)-1-Cyclohexyl-2-((2S,5S)-2,5-dimethyl-pyrrolidin-1-yl)-2-oxo-ethyl]-malonic acid dimethyl ester 

Relevant academic research and scientific papers

Synthesis of the GPR40 partial agonist MK-8666 through a kinetically controlled dynamic enzymatic ketone reduction

A scalable and efficient synthesis of the GPR40 agonist MK-8666 was developed from a simple pyridine building block. The key step to set the stereochemistry at two centers relied on an enzymatic dynamic kinetic reduction of an unactivated ketone. Directed

Platinum(II) Complexes of Functionalized Malonato Ligands: Unequivocal Synthesis, Interaction with a Tetradeoxyribonucleotide and Deoxyribonucleic Acid

The unequivocal syntheses of four cis-> complexes has been achieved, avoiding any interaction between the pendant carboxyl group and the platinum.The complexes have been characterized by elemental analysis, 13C NMR and FAB mass spectroscopy.Their interaction with a tetradeoxyribonucleotide d(T-G-G-T) (G = guanosine, T = ribosylthymine) and DNA (in vitro) has been investigated to show that they form adducts of the type 7,N7'>> as do the known therapeutically activeplatinum complexes.However, the presence of the free carbonyl function increases significantly the reactivity with respect to that of the non-functionalized malonato complexes >.

HIGHLY STEREOSELECTIVE RADICAL ADDITION TO A TRISUBSTITUTED ALKENE BY LOW TEMPERATURE PHOTOLYSIS OF THIOHYDROXAMIC ESTERS

Low temperature carbon radical addition to α,β-unsaturated amides of trans-2,5-dimethylpyrrolidine was achieved in high yield with high diastereoselectivity by photolysis of Barton esters.Use of an olefin substituted with three electron withdrawing groups