1-Propanone, 3-(2-chlorophenyl)-3-hydroxy-1-phenyl-

Base Information

Chemical Name:1-Propanone, 3-(2-chlorophenyl)-3-hydroxy-1-phenyl-
CAS No.:167780-11-2
Molecular Formula:C15H13ClO2
Molecular Weight:260.72
Hs Code.:
DSSTox Substance ID:DTXSID70472412
Nikkaji Number:J2.350.928H
Mol file:167780-11-2.mol

Synonyms:167780-11-2;1-Propanone, 3-(2-chlorophenyl)-3-hydroxy-1-phenyl-;DTXSID70472412

Suppliers and Price of 1-Propanone, 3-(2-chlorophenyl)-3-hydroxy-1-phenyl-

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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price

Total 1 raw suppliers

Chemical Property of 1-Propanone, 3-(2-chlorophenyl)-3-hydroxy-1-phenyl-

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:260.0604073
Heavy Atom Count:18
Complexity:274

Purity/Quality:: 99.90% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)CC(C2=CC=CC=C2Cl)O

Technology Process of 1-Propanone, 3-(2-chlorophenyl)-3-hydroxy-1-phenyl-

There total 9 articles about 1-Propanone, 3-(2-chlorophenyl)-3-hydroxy-1-phenyl- 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: 93.0%

: 65480-18-4,65480-19-5,92428-39-2,132696-74-3
(3-(2-chlorophenyl)oxiran-2-yl)(phenyl)methanone

: 167780-11-2
3-hydroxy-3-(2-chlorophenyl)-1-phenylpropane-1-one

Guidance literature:: With sodium dithionite; sodium carbonate; In water; ethyl acetate; at 20 ℃; for 12h; Irradiation; Inert atmosphere;
DOI:10.1016/j.tetlet.2013.07.112