Dimethyl 2-(4-nitrophenyl)malonate

Base Information

• Chemical Name: Dimethyl 2-(4-nitrophenyl)malonate
• CAS No.: 4033-88-9
• Molecular Formula: C11H11NO6
• Molecular Weight: 253.211
• Hs Code.: 2917399090
• DSSTox Substance ID: DTXSID30377393
• Nikkaji Number: J788.052I
• Wikidata: Q82166591
• Mol file: 4033-88-9.mol

Synonyms:dimethyl 2-(4-nitrophenyl)malonate;4033-88-9;dimethyl 2-(4-nitrophenyl)propanedioate;2-(4-nitrophenyl)malonic acid dimethyl ester;1,3-dimethyl 2-(4-nitrophenyl)propanedioate;dimethyl(4-nitrophenyl)malonate;SCHEMBL3529478;Dimethyl (4-Nitrophenyl)malonate;DTXSID30377393;dimethyl2-(4-nitrophenyl)malonate;PYUABAXAUVLRNX-UHFFFAOYSA-N;MFCD03425806;AKOS005071161;CS-0061798;FT-0680590;7T-0054;A873378

Chemical Property of Dimethyl 2-(4-nitrophenyl)malonate

Chemical Property:

• Melting Point: 125-127oC
• PSA: 98.42000
• LogP: 1.54760
• XLogP3: 1.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 5
• Exact Mass: 253.05863707
• Heavy Atom Count: 18
• Complexity: 313

Purity/Quality:

98%min ^*data from raw suppliers

Dimethyl2-(4-Nitrophenyl)malonate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

Useful:

• Canonical SMILES: COC(=O)C(C1=CC=C(C=C1)[N+](=O)[O-])C(=O)OC

Technology Process of Dimethyl 2-(4-nitrophenyl)malonate

There total 3 articles about Dimethyl 2-(4-nitrophenyl)malonate 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: 78.0%

4-Fluoronitrobenzene (350-46-9,178603-76-4) + malonic acid dimethyl ester (108-59-8) → 2-(4-nitrophenyl)malonic acid dimethyl ester (4033-88-9)

Guidance literature:

With potassium carbonate; In N,N-dimethyl-formamide; at 70 ℃; for 16h;

Reference yield:

para-nitrophenyl bromide (586-78-7) + malonic acid dimethyl ester (108-59-8) → 2-(4-nitrophenyl)malonic acid dimethyl ester (4033-88-9)

Guidance literature:

With potassium phosphate; 4,5-bis(diphenylphosphino)-9,9-dimethylxanthene; palladium diacetate; In 1,4-dioxane; at 90 ℃; for 8h;

Reference yield:

dimethyl 2-phenylmalonate (37434-59-6) → 2-(4-nitrophenyl)malonic acid dimethyl ester (4033-88-9)

Guidance literature:

With sulfuric acid; nitric acid;

upstream raw materials:

dimethyl 2-phenylmalonate

4-Fluoronitrobenzene

malonic acid dimethyl ester

para-nitrophenyl bromide

Downstream raw materials:

dimethyl 2-methyl-2-(4-nitrophenyl)malonate

dimethyl 2-(4-aminophenyl)malonate hydrochloride

2-[2-(2-methoxyethoxy)ethyl]-2-(4-nitrophenyl)malonic acid dimethyl ester

phenyl 4-(1,3-dihydroxy-2-methylpropan-2-yl)phenylcarbamate

Refernces

• 1、 -. "Arylaminoaryl-alkyl-substituted imidazolidine-2,4-diones, process for preparing them, medicaments comprising these compounds, and their use". Page/Page column 76. . Retrieved 2009/09/07.