92828-40-5

Basic information

• Product Name: 1,1,2-Ethanetricarboxylic Acid, 2-(1,1-Dimethylethyl)1,1-Dimethyl Ester
• Synonyms: 1,1,2-Ethanetricarboxylic Acid, 2-(1,1-Dimethylethyl)1,1-Dimethyl Ester;1,1,2-EthanetricarboxylicAcid,2-(1,1-Dimethyleth;TERT-BUTYLOXYCARBOXYLMETHYLMALONATE;2-(tert-Butoxycarbonyl)malonic acid dimethyl ester;1,1,2-Ethanetricarbo
• CAS NO: 92828-40-5
• Molecular Formula: C₁₁H₁₈O₆
• Molecular Weight: 247.26496
• Mol File: 92828-40-5.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,1,2-Ethanetricarboxylic Acid, 2-(1,1-Dimethylethyl)1,1-Dimethyl Ester(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,2-Ethanetricarboxylic Acid, 2-(1,1-Dimethylethyl)1,1-Dimethyl Ester(92828-40-5)
• EPA Substance Registry System: 1,1,2-Ethanetricarboxylic Acid, 2-(1,1-Dimethylethyl)1,1-Dimethyl Ester(92828-40-5)

Safety Data

• Hazardous Substances Data: 92828-40-5(Hazardous Substances Data)

Usage

General Description

1,1,2-Ethanetricarboxylic Acid, 2-(1,1-Dimethylethyl)1,1-Dimethyl Ester is a relatively complex organic compound that partakes in various industrial applications due to its chemical properties. As an ester, it's largely employed in the creation of various polymer products. However, detailed information regarding this specific chemical like the boiling point, melting point, or potential toxicity is not easily accessible, indicating it is not widely used or studied. As with most chemicals, handling should involve appropriate safety measures to prevent direct exposure and potential harm.

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 articles and documents

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

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