2-(3-OXO-CYCLOHEXYL)-MALONIC ACID DIMETHYL ESTER

Base Information

• Chemical Name: 2-(3-OXO-CYCLOHEXYL)-MALONIC ACID DIMETHYL ESTER
• CAS No.: 33646-18-3
• Molecular Formula: C11H16 O5
• Molecular Weight: 228.245
• Hs Code.: 2918300090
• Mol file: 33646-18-3.mol

Synonyms:Cyclohexanemalonicacid, 3-oxo-, dimethyl ester (8CI); Propanedioic acid, (3-oxocyclohexyl)-,dimethyl ester (9CI)

Chemical Property of 2-(3-OXO-CYCLOHEXYL)-MALONIC ACID DIMETHYL ESTER

Chemical Property:

• Boiling Point: 306.5°Cat760mmHg
• Flash Point: 132°C
• PSA: 69.67000
• Density: 1.17g/cm³
• LogP: 0.70790

Purity/Quality:

99% ^*data from raw suppliers

2-(3-OXO-CYCLOHEXYL)-MALONIC ACID DIMETHYL ESTER 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of 2-(3-OXO-CYCLOHEXYL)-MALONIC ACID DIMETHYL ESTER

There total 5 articles about 2-(3-OXO-CYCLOHEXYL)-MALONIC ACID DIMETHYL ESTER which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%

cyclohexenone (930-68-7) + malonic acid dimethyl ester (108-59-8) → dimethyl 2-(3-oxocyclohexyl)malonate (33646-18-3)

Guidance literature:

(anthracenebisresorcinol^(4-):2La⁽³⁺⁾)polymer; In benzene; at 20 ℃; for 48h;

DOI:10.1246/cl.1999.797

Reference yield: 98.0%

cyclohexenone (930-68-7) + diethyl malonate (105-53-3) → dimethyl 2-(3-oxocyclohexyl)malonate (33646-18-3)

Guidance literature:

Mg-La mixed oxides; In N,N-dimethyl-formamide; at 24.85 ℃; for 4h;

DOI:10.1002/adsc.200404371

Reference yield: 87.0%

→ dimethyl 2-(3-oxocyclohexyl)malonate (33646-18-3)

Guidance literature:

With benzoic acid; In ethyl acetate; at 30 ℃; for 24h; enantioselective reaction;

upstream raw materials:

cyclohexenone

malonic acid dimethyl ester

diazomethane

(3-oxocyclohexyl)malonic acid

Downstream raw materials:

2-{3-[bis-(4-hydroxy-phenyl)-methylene]-cyclohexyl}-malonic acid dimethyl ester

(3-oxocyclohexyl)malonic acid

dimethyl 2-(4-bromobut-2-yn-1-yl)-2-(3-oxocyclohexyl)malonate

3-(2-methanesulfonyloxyethyl)[bis(4-methoxymethoxyphenyl)methylene]cyclohexane

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