3-(2-Chlorophenyl)-2-oxopropyl Acetate

Base Information

Chemical Name:3-(2-Chlorophenyl)-2-oxopropyl Acetate
CAS No.:851547-69-8
Molecular Formula:C11H11ClO3
Molecular Weight:226.66
Hs Code.:
DSSTox Substance ID:DTXSID60582751
Wikidata:Q82474246

Synonyms:3-(2-Chlorophenyl)-2-oxopropyl Acetate;851547-69-8;SCHEMBL2250581;DTXSID60582751;HOZFGIZZOORECQ-UHFFFAOYSA-N

Suppliers and Price of 3-(2-Chlorophenyl)-2-oxopropyl Acetate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 3-(2-Chlorophenyl)-2-oxopropyl Acetate

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:226.0396719
Heavy Atom Count:15
Complexity:240

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)OCC(=O)CC1=CC=CC=C1Cl

Technology Process of 3-(2-Chlorophenyl)-2-oxopropyl Acetate

There total 3 articles about 3-(2-Chlorophenyl)-2-oxopropyl Acetate 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: 43.0%

: 128426-51-7
1-chloro-3-(2-chlorophenyl)propan-2-one

: 64-19-7,77671-22-8
acetic acid

: 851547-69-8
3-(2-chlorophenyl)-2-oxopropyl acetate

Guidance literature:: With triethylamine; In acetone; at 20 ℃;
DOI:10.1021/jm060631p

Reference yield: 43.0%

: 851547-69-8
3-(2-chlorophenyl)-2-oxopropyl acetate

Guidance literature:

Reference yield:

: 312624-11-6
(2-chlorobenzyl)zinc(II) chloride

: 851547-69-8
3-(2-chlorophenyl)-2-oxopropyl acetate

Guidance literature:: Multi-step reaction with 2 steps

1: 22 percent / Pd(PPh₃)4 / N,N-dimethyl-acetamide / 20 °C

2: 43 percent / Et₃N / acetone / 20 °C

With triethylamine; tetrakis(triphenylphosphine) palladium⁽⁰⁾; In N,N-dimethyl acetamide; acetone;
DOI:10.1021/jm060631p