2-Phenyl-1,3-cyclopentanedione

Base Information

Chemical Name:2-Phenyl-1,3-cyclopentanedione
CAS No.:6853-01-6
Molecular Formula:C11H10O2
Molecular Weight:174.19600
Hs Code.:
ChEMBL ID:CHEMBL280712
DSSTox Substance ID:DTXSID90531272
Nikkaji Number:J2.495.039E
Wikidata:Q82403011

Synonyms:2-phenyl-1,3-cyclopentanedione;2-Phenylcyclopentane-1,3-dione;6853-01-6;CHEMBL280712;SCHEMBL5315718;DTXSID90531272;2-Phenyl-cyclopentane-1,3-dione

Suppliers and Price of 2-Phenyl-1,3-cyclopentanedione

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 2 raw suppliers

Chemical Property of 2-Phenyl-1,3-cyclopentanedione

Chemical Property:

PSA：34.14000
LogP:1.70220
XLogP3:1.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:174.068079557
Heavy Atom Count:13
Complexity:210

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC(=O)C(C1=O)C2=CC=CC=C2

Technology Process of 2-Phenyl-1,3-cyclopentanedione

There total 5 articles about 2-Phenyl-1,3-cyclopentanedione 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: 80.0%

: 936-51-6
2-phenyl-1,3-dioxolane

: 17082-61-0
1,2-bis(trimethylsiloxy)cyclobutene

: 6853-01-6
2-phenylcyclopentane-1,3-dione

Guidance literature:: With boron trifluoride diethyl etherate; In dichloromethane; -78 deg C, 8 h; RT, overnight;

Reference yield:

: 1589-82-8
phenylmagnesium bromide

: 6853-01-6
2-phenylcyclopentane-1,3-dione

Guidance literature:: Multi-step reaction with 2 steps

1: copper(l) iodide / tetrahydrofuran / 3 h / 0 - 25 °C / Inert atmosphere; Schlenk technique

2: sodium ethanolate / diethyl ether / 2 h / Inert atmosphere; Schlenk technique; Reflux

With copper(l) iodide; sodium ethanolate; In tetrahydrofuran; diethyl ether;
DOI:10.1002/anie.201706763