1,5-Pentanedione, 3-(4-nitrophenyl)-1,5-diphenyl-

Base Information

Chemical Name:1,5-Pentanedione, 3-(4-nitrophenyl)-1,5-diphenyl-
CAS No.:113451-18-6
Molecular Formula:C23H19NO4
Molecular Weight:373.408
Hs Code.:
DSSTox Substance ID:DTXSID30475641
Nikkaji Number:J2.490.357E
Wikidata:Q82306295

Synonyms:1,5-Pentanedione, 3-(4-nitrophenyl)-1,5-diphenyl-;113451-18-6;DTXSID30475641

Suppliers and Price of 1,5-Pentanedione, 3-(4-nitrophenyl)-1,5-diphenyl-

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
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Total 0 raw suppliers

Chemical Property of 1,5-Pentanedione, 3-(4-nitrophenyl)-1,5-diphenyl-

Chemical Property:

XLogP3:4.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:7
Exact Mass:373.13140809
Heavy Atom Count:28
Complexity:503

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)CC(CC(=O)C2=CC=CC=C2)C3=CC=C(C=C3)[N+](=O)[O-]

Technology Process of 1,5-Pentanedione, 3-(4-nitrophenyl)-1,5-diphenyl-

There total 7 articles about 1,5-Pentanedione, 3-(4-nitrophenyl)-1,5-diphenyl- 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: 64.0%

: 1222-98-6
4-nitrochalcone

: 98-86-2
acetophenone

: 113451-18-6
3-(p-nitrophenyl)-1,5-diphenyl-1,5-pentanedione

Guidance literature:: 4-nitrochalcone; acetophenone; With trimethyl orthoformate; In tetrachloromethane; for 0.0833333h;

With trifluorormethanesulfonic acid; In tetrachloromethane; at 20 ℃;
DOI:10.1039/C6NJ02954J