57293-62-6

Basic information

• Product Name: 2,5-Dioxo-bicyclo[2.2.2]octane-1,4-dicarboxylic acid diMethyl ester
• Synonyms: 2,5-Dioxo-bicyclo[2.2.2]octane-1,4-dicarboxylic acid diMethyl ester;Dimethyl 2,5-dioxo-bicyclo[2,2,2]octane-1,4-dicarboxylate
• CAS NO: 57293-62-6
• Molecular Formula: C₁₂H₁₄O₆
• Molecular Weight: 254.23596
• EINECS: -0
• Mol File: 57293-62-6.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2,5-Dioxo-bicyclo[2.2.2]octane-1,4-dicarboxylic acid diMethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5-Dioxo-bicyclo[2.2.2]octane-1,4-dicarboxylic acid diMethyl ester(57293-62-6)
• EPA Substance Registry System: 2,5-Dioxo-bicyclo[2.2.2]octane-1,4-dicarboxylic acid diMethyl ester(57293-62-6)

Safety Data

• Hazardous Substances Data: 57293-62-6(Hazardous Substances Data)

Usage

General Description

2,5-Dioxo-bicyclo[2.2.2]octane-1,4-dicarboxylic acid dimethyl ester is a complex organic compound. It is a diester derivative of a bicyclic diketopiperazine, which is a class of compounds with potential bioactivity. This chemical is primarily used in research settings as a building block for the synthesis of various organic compounds with potential pharmaceutical applications. Its unique structure and functional groups make it suitable for use as a starting material in the development of new drugs and medicinal compounds. However, due to its complexity and potential reactivity, it must be handled and used with care under controlled conditions by trained professionals.

Upstream product

• 6289-46-9 dimethyl 2,5-dioxocyclohexane-1,4-dicarboxylate 
• 106-93-4 ethylene dibromide 

Downstream Products

• 711-02-4 1,4-bicyclo[2.2.2]octanedicarboxylic acid 
• 18720-35-9 bicyclo[2.2.2]octane-1,4-dicarboxylic acid monomethyl ester 
• 1459-96-7 dimethyl bicyclo[2.2.2]octane-1,4-dicarboxylate 

Relevant articles and documents

Bicyclo [2.2.2] octane - 1, 4 - dicarboxylic acid mono methyl ester synthesis method

The invention relates to a synthetic method of an organic compound. The synthetic method of bicyclo-[2.2.2]octane-1,4-dicarboxylic acid monomethyl easter is as follows: firstly, adopting sodium hydride, DMSS and 1,2-dibromoethane to synthesize the intermediate I; secondly, adopting the intermediate I, sodium acetate, ammourea hydrochloride and alcohol to synthesize semicarbazon; thirdly, adopting potassium hydroxide, diethylene glycol and semicarbazon to synthesize target diacid; fourthly, adopting target diacid, thionyl chloride and methanol to synthesize target diester; and fifthly, adopting target diester, potassium hydroxide and 95% of methanol water solution to synthesize the target product monoester. The invention has reasonable synthetic process route, mild process conditions, environment friendly, easy operation, low raw material cost, high product yield and excellent purity, and is applicable to industrial production and satisfies the application requirement of each industry.

Chemoenzymatic synthesis and application of bicyclo [2.2.2] octadiene ligands: Increased efficiency in rhodium-catalyzed asymmetric conjugate additions by electronic tuning

(Figure Presented) On your bi(cycle)kel A series of 1,4dimethyl bicyclic [2.2.2] diene ligands with tunable substitution at the bridge positions was accessed using a lipase resolution and a high yielding six step sequence (see scheme). The bridgehead meth

Rodlike molecules by Kolbe electrolysis

A new short and simple pathway to rigid, rod-shaped hydrocarbon skeletons, in particular of the oligo-bicyclo[2.2.2]octane type, is described. The key step consists of an electrochemical C-C bond coupling reaction between bridgehead positions of bi- and tricyclic carboxylic acids. Functional groups can be retained, they influence the yield of the C-C bond connection. In this way, otherwise difficult or laborious syntheses are shortened, and rigid, non-collapsable nano size spacer units are easily available. The optimized electrochemical procedures are described in detail.