(E)-3-(4-chlorobenzylidene)indolin-2-one

Base Information

Chemical Name:(E)-3-(4-chlorobenzylidene)indolin-2-one
CAS No.:29551-52-8
Molecular Formula:C15H10ClNO
Molecular Weight:255.703
Hs Code.:
Mol file:29551-52-8.mol

Synonyms:3-[1-(4-Chloro-phenyl)-meth-(E)-ylidene]-1,3-dihydro-indol-2-one;(E)-3-(4-Chlorobenzylidene)indolin-2-one;3-((E)-4-chloro-benzylidene)-indolin-2-one;3-((E)-4-Chlor-benzyliden)-indolin-2-on;(E)-3-(4-Chlor-benzyliden)-oxindol;3-[(4-chlorophenyl)methylidene]-1,3-dihydro-2H-indol-2-one;

Suppliers and Price of (E)-3-(4-chlorobenzylidene)indolin-2-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 4 raw suppliers

Chemical Property of (E)-3-(4-chlorobenzylidene)indolin-2-one

Chemical Property:

PSA：29.10000
LogP:3.97070

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of (E)-3-(4-chlorobenzylidene)indolin-2-one

There total 8 articles about (E)-3-(4-chlorobenzylidene)indolin-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: 95.0%

: 59-48-3
2-oxoindole

: 104-86-9
4-chlorobenzylamine

: 29551-52-8
3-[(E)-(4-chlorophenyl)methylidene]-1,3-dihydro-2H-indol-2-one

Guidance literature:: With oxygen; iron(II) bromide; at 100 ℃; for 16h; Schlenk technique;
DOI:10.1002/ejoc.202001300

Reference yield: 92.0%

: 59-48-3
2-oxoindole

: 104-88-1
4-chlorobenzaldehyde

: 29551-52-8
3-[(E)-(4-chlorophenyl)methylidene]-1,3-dihydro-2H-indol-2-one

Guidance literature:: With 1-deoxy-1-(methylamino)-D-glucitol; In ethanol; water; at 78 ℃; for 0.833333h; Solvent; Temperature; stereoselective reaction; Catalytic behavior;
DOI:10.2174/1570178615666181030095728

Reference yield: 78.0%

: 104-88-1
4-chlorobenzaldehyde

: 152302-94-8
N-(2-Iodophenyl)-α-(diethoxyphosphinyl)acetamide

: 29551-52-8
3-[(E)-(4-chlorophenyl)methylidene]-1,3-dihydro-2H-indol-2-one

Guidance literature:: With tetrakis(triphenylphosphine) palladium⁽⁰⁾; caesium carbonate; In tetrahydrofuran; at 100 ℃; for 1h; Inert atmosphere; Microwave irradiation;
DOI:10.1016/j.tet.2010.03.018