1,5-Dibenzoyl-1,3-cyclopentadiene

Base Information

Chemical Name:1,5-Dibenzoyl-1,3-cyclopentadiene
CAS No.:201138-71-8
Molecular Formula:C₁₉H₁₄O₂
Molecular Weight:274.319
Hs Code.:
European Community (EC) Number:633-821-3

Synonyms:1,5-DIBENZOYL-1,3-CYCLOPENTADIENE;SCHEMBL13985151;AKOS024322227

Suppliers and Price of 1,5-Dibenzoyl-1,3-cyclopentadiene

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

Sigma-Aldrich
1,5-DIBENZOYL-1,3-CYCLOPENTADIENE Aldrich
1ea
$ 144.00

Total 1 raw suppliers

Chemical Property of 1,5-Dibenzoyl-1,3-cyclopentadiene

Chemical Property:

Boiling Point:447.5±45.0 °C(Predicted)
Density:1.206±0.06 g/cm3(Predicted)
XLogP3:4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:274.099379685
Heavy Atom Count:21
Complexity:460

Purity/Quality:

98%,99%, ^*data from raw suppliers

1,5-DIBENZOYL-1,3-CYCLOPENTADIENE Aldrich ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)C2C=CC=C2C(=O)C3=CC=CC=C3

Technology Process of 1,5-Dibenzoyl-1,3-cyclopentadiene

There total 3 articles about 1,5-Dibenzoyl-1,3-cyclopentadiene 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: 62.0%

: 98-88-4
benzoyl chloride

: 946-02-1
4-chlorobutyl benzoate

: 201138-71-8
1,5-dibenzoylcyclopentadiene

Guidance literature:: With bis(η⁵-cyclopentadienyl)yttrium(III) chloride; In tetrahydrofuran; for 11h; Mechanism; Ambient temperature; other acyl chlorides, var. reaction time;
DOI:10.1016/0022-328X(91)86041-N