1-(4-Methoxyphenyl)-7-phenyl-1,4,6-heptatrien-3-one

Base Information

• Chemical Name: 1-(4-Methoxyphenyl)-7-phenyl-1,4,6-heptatrien-3-one
• CAS No.: 622-70-8
• Molecular Formula: C₂₀H₁₈O₂
• Molecular Weight: 290.362
• European Community (EC) Number: 653-550-4
• DSSTox Substance ID: DTXSID601225100
• ChEMBL ID: CHEMBL1885065

Synonyms:1-(4-METHOXYPHENYL)-7-PHENYL-1,4,6-HEPTATRIEN-3-ONE;622-70-8;MLS002639416;Anisalcinnamalaceton;CHEMBL1885065;DTXSID601225100;HMS3092A09;AKOS024333532;SMR001548860

Chemical Property of 1-(4-Methoxyphenyl)-7-phenyl-1,4,6-heptatrien-3-one

Chemical Property:

• Vapor Pressure: 1.67E-09mmHg at 25°C
• Boiling Point: 483.5°Cat760mmHg
• Flash Point: 214.4°C
• Density: 1.101g/cm³
• XLogP3: 4.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 6
• Exact Mass: 290.130679813
• Heavy Atom Count: 22
• Complexity: 405

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)C=CC(=O)C=CC=CC2=CC=CC=C2

Technology Process of 1-(4-Methoxyphenyl)-7-phenyl-1,4,6-heptatrien-3-one

There total 6 articles about 1-(4-Methoxyphenyl)-7-phenyl-1,4,6-heptatrien-3-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:

1-phenyl-1,3-hexadien-5-one (4173-44-8) + 4-methoxy-benzaldehyde (123-11-5) → 1-(4-methoxy-phenyl)-7-phenyl-hepta-1,4,6-trien-3-one (622-70-8)

Guidance literature:

With potassium hydroxide;

Reference yield:

3-phenyl-propenal (104-55-2) → 1-(4-methoxy-phenyl)-7-phenyl-hepta-1,4,6-trien-3-one (622-70-8)

Guidance literature:

Multi-step reaction with 2 steps

1: alkali

2: alcoholic KOH-solution

With potassium hydroxide;

Reference yield:

3-phenyl-propenal (104-55-2) + 4-(4-methoxyphenyl)-3-buten-2-one (3815-30-3) → 1-(4-methoxy-phenyl)-7-phenyl-hepta-1,4,6-trien-3-one (622-70-8)

Guidance literature:

With potassium hydroxide;

upstream raw materials:

1-phenyl-1,3-hexadien-5-one

4-methoxy-benzaldehyde

3-phenyl-propenal

4-(4-methoxyphenyl)-3-buten-2-one

Downstream raw materials:

2-(4-methoxy-phenyl)-4-oxo-6-styryl-cyclohexane-1,1-dicarboxylic acid dimethyl ester

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