(3E)-3-[(4-Chlorophenyl)imino]butan-2-one

Base Information

• Chemical Name: (3E)-3-[(4-Chlorophenyl)imino]butan-2-one
• CAS No.: 87277-48-3
• Molecular Formula: C10H10ClNO
• Molecular Weight: 195.648
• DSSTox Substance ID: DTXSID30515652
• Mol file: 87277-48-3.mol

Synonyms:87277-48-3;(3E)-3-[(4-Chlorophenyl)imino]butan-2-one;DTXSID30515652

Chemical Property of (3E)-3-[(4-Chlorophenyl)imino]butan-2-one

Chemical Property:

• XLogP3: 2.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 195.0450916
• Heavy Atom Count: 13
• Complexity: 217

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of (3E)-3-[(4-Chlorophenyl)imino]butan-2-one

There total 1 articles about (3E)-3-[(4-Chlorophenyl)imino]butan-2-one 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:

4-chloro-aniline (106-47-8) + dimethylglyoxal (431-03-8) → 3-[(E)-4-Chloro-phenylimino]-butan-2-one (87277-48-3)

Guidance literature:

With acetic acid; In methanol; at 20 ℃;

DOI:10.1002/hc.21424

Reference yield: 48.0%

3-[(E)-4-Chloro-phenylimino]-butan-2-one (87277-48-3) + 1,4-phenylenediamine (106-50-3) → C26H24Cl2N4

Guidance literature:

In methanol; at 20 ℃;

DOI:10.1002/hc.21424

Reference yield: 40.0%

3-[(E)-4-Chloro-phenylimino]-butan-2-one (87277-48-3) + benzohydroximoyl chloride (698-16-8) → 1-[4-(4-Chloro-phenyl)-5-methyl-3-phenyl-4,5-dihydro-[1,2,4]oxadiazol-5-yl]-ethanone (87277-34-7)

Guidance literature:

With triethylamine; In toluene; for 5h; Ambient temperature;

DOI:10.1055/s-1983-30395

upstream raw materials:

4-chloro-aniline

dimethylglyoxal

Downstream raw materials:

1-[4-(4-Chloro-phenyl)-5-methyl-3-phenyl-4,5-dihydro-[1,2,4]oxadiazol-5-yl]-ethanone