1-(2-Chlorophenyl)-3-methyl-1-butanone

Base Information

Chemical Name:1-(2-Chlorophenyl)-3-methyl-1-butanone
CAS No.:348168-03-6
Molecular Formula:C₁₁H₁₃ClO
Molecular Weight:196.677
Hs Code.:
European Community (EC) Number:810-052-3

Synonyms:348168-03-6;1-(2-Chlorophenyl)-3-methyl-1-butanone;1-(2-chlorophenyl)-3-methylbutan-1-one;1-(2-Chloro-phenyl)-3-methyl-butan-1-one;SCHEMBL11650545;MFCD12824574;AKOS010258675;AS-46778;DB-215468;CS-0332698;F10466

Suppliers and Price of 1-(2-Chlorophenyl)-3-methyl-1-butanone

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 4 raw suppliers

Chemical Property of 1-(2-Chlorophenyl)-3-methyl-1-butanone

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:196.0654927
Heavy Atom Count:13
Complexity:177

Purity/Quality:: 98%+ ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C)CC(=O)C1=CC=CC=C1Cl

Technology Process of 1-(2-Chlorophenyl)-3-methyl-1-butanone

There total 3 articles about 1-(2-Chlorophenyl)-3-methyl-1-butanone 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:

active charcoal: active charcoal

: 108-73-6
3,5-dihydroxyphenol

: 108-12-3
isopentanoyl chloride

: 348168-03-6
chloroisovalerophenone

Guidance literature:: With hydrogenchloride; aluminium chloride; In dichloromethane; ethyl acetate; nitrobenzene;

Reference yield:

: 289686-74-4
2‐chloro‐N‐methoxy‐N‐methylbenzamide

: 920-36-5,90269-51-5
(2-methylpropyl)lithium

: 348168-03-6
chloroisovalerophenone

Guidance literature:: In tetrahydrofuran; at -78 ℃; for 0.5h;
DOI:10.1021/acs.orglett.0c01085

Reference yield:

: 609-65-4
o-chlorobenzoyl chloride

: 348168-03-6
chloroisovalerophenone

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / dichloromethane / 0 - 20 °C

2: tetrahydrofuran / 0.5 h / -78 °C

With pyridine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/acs.orglett.0c01085