5-[(2,3-Dichlorophenyl)methylidene]pyrimidine-2,4,6(1H,3H,5H)-trione

Base Information

• Chemical Name: 5-[(2,3-Dichlorophenyl)methylidene]pyrimidine-2,4,6(1H,3H,5H)-trione
• CAS No.: 148119-29-3
• Molecular Formula: C11H6Cl2N2O3
• Molecular Weight: 285.086
• DSSTox Substance ID: DTXSID70576247
• Mol file: 148119-29-3.mol

Synonyms:148119-29-3;5-[(2,3-Dichlorophenyl)methylidene]pyrimidine-2,4,6(1H,3H,5H)-trione;DTXSID70576247;AKOS024388572

Chemical Property of 5-[(2,3-Dichlorophenyl)methylidene]pyrimidine-2,4,6(1H,3H,5H)-trione

Chemical Property:

• XLogP3: 2.2
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 1
• Exact Mass: 283.9755474
• Heavy Atom Count: 18
• Complexity: 414

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C(=C1)Cl)Cl)C=C2C(=O)NC(=O)NC2=O

Technology Process of 5-[(2,3-Dichlorophenyl)methylidene]pyrimidine-2,4,6(1H,3H,5H)-trione

There total 1 articles about 5-[(2,3-Dichlorophenyl)methylidene]pyrimidine-2,4,6(1H,3H,5H)-trione 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: 85.0%

BARBITURIC ACID (67-52-7,944357-77-1) + 2,3-dichlorobenzylaldehyde (6334-18-5) → 5-(2,3-dichlorobenzylidene)barbituric acid (148119-29-3)

Guidance literature:

In water; Heating;

DOI:10.1002/jhet.5570400106

Reference yield: 70.0%

benzyl bromide (100-39-0) + 5-(2,3-dichlorobenzylidene)barbituric acid (148119-29-3) → 5-[1-(2,3-dichlorophenyl)-2-phenylethyl]barbituric acid (538353-45-6)

Guidance literature:

With zinc; In tetrahydrofuran; at 0 - 30 ℃;

DOI:10.1002/jhet.5570400106

Reference yield:

5-(2,3-dichlorobenzylidene)barbituric acid (148119-29-3) → 5-[1-(2,3-dichlorophenyl)-2-phenylethyl]-2,4,6-trichloropyrimidine

Guidance literature:

Multi-step reaction with 2 steps

1: 70 percent / zinc / tetrahydrofuran / 0 - 30 °C

2: 52 percent / phosphorus oxychloride; phosphorus pentachloride / Heating

With phosphorus pentachloride; zinc; trichlorophosphate; In tetrahydrofuran;

DOI:10.1002/jhet.5570400106

upstream raw materials:

BARBITURIC ACID

2,3-dichlorobenzylaldehyde

Downstream raw materials:

5-[1-(2,3-dichlorophenyl)-2-phenylethyl]barbituric acid