Ethanimidoyl chloride, N-(4-chlorophenyl)-

Base Information

• Chemical Name: Ethanimidoyl chloride, N-(4-chlorophenyl)-
• CAS No.: 76540-13-1
• Molecular Formula: C8H7Cl2N
• Molecular Weight: 188.056
• DSSTox Substance ID: DTXSID70479562

Synonyms:Ethanimidoyl chloride, N-(4-chlorophenyl)-;76540-13-1;DTXSID70479562

Chemical Property of Ethanimidoyl chloride, N-(4-chlorophenyl)-

Chemical Property:

• XLogP3: 3.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 1
• Rotatable Bond Count: 1
• Exact Mass: 186.9955546
• Heavy Atom Count: 11
• Complexity: 148

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC(=NC1=CC=C(C=C1)Cl)Cl

Technology Process of Ethanimidoyl chloride, N-(4-chlorophenyl)-

There total 1 articles about Ethanimidoyl chloride, N-(4-chlorophenyl)- 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:

N-(4-chlorophenyl)acetamide (539-03-7) → N-(1-chloroethylidene)-4-chlorobenzenamine (76540-13-1)

Guidance literature:

With phosphorus pentachloride;

Reference yield: 63.0%

N-(1-chloroethylidene)-4-chlorobenzenamine (76540-13-1) → 1,4-bis(4-chlorophenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene (19215-48-6)

Guidance literature:

With potassium tellurocyanate; In dimethyl sulfoxide; at 20 ℃; for 2.5h; Inert atmosphere;

DOI:10.1080/10426507.2014.902830

Reference yield: 29.0%

2-Picolinic acid (98-98-6) + N-(1-chloroethylidene)-4-chlorobenzenamine (76540-13-1) → Pyridine-2-carboxylic acid acetyl-(4-chloro-phenyl)-amide (76540-05-1)

Guidance literature:

With triethylamine; In acetonitrile;

upstream raw materials:

N-(4-chlorophenyl)acetamide

Downstream raw materials:

Pyridine-2-carboxylic acid acetyl-(4-chloro-phenyl)-amide

C₁₄H₁₁ClN₂O₂*ClH

1,4-bis(4-chlorophenyl)-2,3-dimethyl-1,4-diaza-1,3-butadiene

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