(2E)-1-(4-aminophenyl)-3-biphenyl-4-ylprop-2-en-1-one

Base Information

• Chemical Name: (2E)-1-(4-aminophenyl)-3-biphenyl-4-ylprop-2-en-1-one
• CAS No.: 899588-25-1
• Molecular Formula: C₂₁H₁₇NO
• Molecular Weight: 299.372
• Mol file: 899588-25-1.mol

Synonyms:(2E)-1-(4-aminophenyl)-3-biphenyl-4-ylprop-2-en-1-one;(E)-1-(4-aminophenyl)-3-(4-phenylphenyl)prop-2-en-1-one

Chemical Property of (2E)-1-(4-aminophenyl)-3-biphenyl-4-ylprop-2-en-1-one

Chemical Property:

Purity/Quality:

98%min ^*data from raw suppliers

(2E)-1-(4-Aminophenyl)-3-biphenyl-4-yl-prop-2-en-1-one ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of (2E)-1-(4-aminophenyl)-3-biphenyl-4-ylprop-2-en-1-one

There total 2 articles about (2E)-1-(4-aminophenyl)-3-biphenyl-4-ylprop-2-en-1-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:

p-aminobenzophenone (99-92-3) + 4-Phenylbenzaldehyde (3218-36-8) → C21H17NO (899588-25-1)

Guidance literature:

p-aminobenzophenone; With potassium hydroxide; In ethanol; at 0 ℃;

4-Phenylbenzaldehyde; In ethanol;

DOI:10.1039/c4md00371c

Reference yield:

p-aminobenzophenone (99-92-3) + 4-Phenylbenzaldehyde (3218-36-8) → C21H17NO (899588-25-1)

Guidance literature:

With sodium hydroxide; In ethanol; at 20 ℃;

DOI:10.1080/14756366.2019.1615485

Reference yield:

3-bromo-2,3-dihydro-2,2-dimethylnaphtho[1,2-b]furan-4,5-dione (83280-64-2) + C21H17NO (899588-25-1) → (E)-3-(4-(3-(biphenyl-4-yl)acryloyl)phenylamino)-2,2-dimethyl-2,3-dihydronaphtho[1,2-b]furan-4,5-dione

Guidance literature:

In dichloromethane; at 20 ℃;

DOI:10.1039/c4md00371c

upstream raw materials:

p-aminobenzophenone

4-Phenylbenzaldehyde