Dichloromethyl 2,2-di-chlorovinyl ketone

Base Information

• Chemical Name: Dichloromethyl 2,2-di-chlorovinyl ketone
• CAS No.: 10561-99-6
• Molecular Formula: C4H2Cl4O
• Molecular Weight: 207.871
• DSSTox Substance ID: DTXSID801023407
• Mol file: 10561-99-6.mol

Synonyms:10561-99-6;dichloromethyl 2,2-di-chlorovinyl ketone;DTXSID801023407;1,1,4,4-tetrachloro-3-buten-2-one

Chemical Property of Dichloromethyl 2,2-di-chlorovinyl ketone

Chemical Property:

• XLogP3: 3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 2
• Exact Mass: 207.883025
• Heavy Atom Count: 9
• Complexity: 136

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(=C(Cl)Cl)C(=O)C(Cl)Cl

Technology Process of Dichloromethyl 2,2-di-chlorovinyl ketone

There total 1 articles about Dichloromethyl 2,2-di-chlorovinyl ketone 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:

1,1,3,4-tetrachloro-1,3-butadiene (42769-38-0) → 1,1,4,4-tetrachloro-1-buten-3-one (10561-99-6) + oxalic acid (144-62-7,97993-78-7)

Guidance literature:

With nitric acid; 50-60 deg C for 5 hours then left overnight;

Reference yield: 93.0%

1,1,4,4-tetrachloro-1-buten-3-one (10561-99-6) + 1-amino-3-methylbenzene (108-44-1) → 4,4-dichloro-1,1-di-1-buten-3-one (84114-95-4)

Guidance literature:

In diethyl ether; for 1h; Heating;

Reference yield: 90.5%

1,1,4,4-tetrachloro-1-buten-3-one (10561-99-6) + aniline (62-53-3) → 4,4-dichloro-1,1-dianilino-1-buten-3-one (10562-03-5)

Guidance literature:

In diethyl ether; for 1h; Heating;

upstream raw materials:

1,1,3,4-tetrachloro-1,3-butadiene

Downstream raw materials:

C₁₆H₁₂Cl₃O₂P

4,4-dichloro-1,1-dianilino-1-buten-3-one

4,4-dichloro-1,1-di-1-buten-3-one

4,4-dichloro-1,1-di-1-buten-3-one

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