1,2,3-Triphenylpropane-1,3-dione

Base Information

Chemical Name:1,2,3-Triphenylpropane-1,3-dione
CAS No.:4888-39-5
Molecular Formula:C21H16O2
Molecular Weight:300.357
Hs Code.:
DSSTox Substance ID:DTXSID30392768
Nikkaji Number:J2.034.112B
Wikidata:Q82191164
ChEMBL ID:CHEMBL264072
Mol file:4888-39-5.mol

Synonyms:1,2,3-triphenylpropane-1,3-dione;phenyldibenzoylmethane;4888-39-5;CHEMBL264072;SCHEMBL1667152;DTXSID30392768;SJMBKGWSQZFQRI-UHFFFAOYSA-N;1,2,3-Triphenyl-1,3-propanedione

Suppliers and Price of 1,2,3-Triphenylpropane-1,3-dione

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 1 raw suppliers

Chemical Property of 1,2,3-Triphenylpropane-1,3-dione

Chemical Property:

XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:300.115029749
Heavy Atom Count:23
Complexity:366

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(C(=O)C2=CC=CC=C2)C(=O)C3=CC=CC=C3

Technology Process of 1,2,3-Triphenylpropane-1,3-dione

There total 41 articles about 1,2,3-Triphenylpropane-1,3-dione 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: 56.0%

: 479-33-4
2,3,4,5-tetraphenylcyclopenta-2,4-dienone

: 4888-39-5
1,2,3-triphenylpropane-1,3-dione

: 79255-64-4
5-(Benzoyloxy)-3,4,5-triphenyl-1-oxacyclopent-3-en-2-one

Guidance literature:: With ozone; In dichloromethane; at -78 ℃; Mechanism;
DOI:10.1021/jo00337a050

Reference yield: 55.0%

: 591-50-4
iodobenzene

: 120-46-7,61346-73-4
1,3-diphenylpropanedione

: 4888-39-5
1,2,3-triphenylpropane-1,3-dione

Guidance literature:: With copper(l) iodide; potassium carbonate; L-proline; In dimethyl sulfoxide; at 90 ℃; for 48h; Inert atmosphere;
DOI:10.1002/ejoc.201601513

Reference yield: 45.0%

: 2-chloro-1,2-diphenyl-2-[(4-tolyl)sulfinyl]ethanol

: 98-88-4
benzoyl chloride

: 4888-39-5
1,2,3-triphenylpropane-1,3-dione

Guidance literature:: 2-chloro-1,2-diphenyl-2-[(4-tolyl)sulfinyl]ethanol; With tert-butylmagnesium chloride; In tetrahydrofuran; at -45 ℃; for 0.166667h; Inert atmosphere;

With isopropylmagnesium chloride; In tetrahydrofuran; at -45 - 20 ℃; for 1.7h; Inert atmosphere;

benzoyl chloride; In tetrahydrofuran; at 20 ℃; for 1.5h; Inert atmosphere;
DOI:10.1055/s-0031-1260251