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4'-CHLORO-3-(4-FLUOROPHENYL)PROPIOPHENONE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

654673-24-2

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654673-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 654673-24-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,5,4,6,7 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 654673-24:
(8*6)+(7*5)+(6*4)+(5*6)+(4*7)+(3*3)+(2*2)+(1*4)=182
182 % 10 = 2
So 654673-24-2 is a valid CAS Registry Number.
InChI:InChI=1/C15H12ClFO/c16-13-6-4-12(5-7-13)15(18)10-3-11-1-8-14(17)9-2-11/h1-2,4-9H,3,10H2

654673-24-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chlorophenyl)-3-(4-fluorophenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names 4'-CHLORO-3-(4-FLUOROPHENYL)PROPIOPHENONE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:654673-24-2 SDS

654673-24-2Downstream Products

654673-24-2Relevant academic research and scientific papers

Iron-Catalyzed α-Alkylation of Ketones with Alcohols

Elangovan, Saravanakumar,Sortais, Jean-Baptiste,Beller, Matthias,Darcel, Christophe

supporting information, p. 14483 - 14486 (2016/01/25)

A general and benign iron-catalyzed α-alkylation reaction of ketones with primary alcohols has been developed. The key to success of the reaction is the use of a Kn?lker-type complex as catalyst (2 mol %) in the presence of Cs2CO3 as base (10 mol %) under hydrogen-borrowing conditions. Using 2-aminobenzyl alcohol as alkylation reagent allows for the "green" synthesis of quinoline derivatives.

Selective 1,4-reduction of chalcones with Zn/NH4Cl/C 2H5OH/H2O

Li, Jian-Ping,Zhang, Yong-Xia,Ji, Yan

, p. 390 - 393 (2008/12/20)

In this paper, the Zn/NH4Cl/C2H5OH/H 2O system was applied for the selective 1,4-reduction of chalcones undermild conditions with high selectivity. Themerit lies in inexpensive reagent, simple operation and envi

CHEMICAL COMPOUNDS

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Page 88, (2010/02/06)

Compounds of formula (I):wherein variable groups are as defined within; for use in the inhibition of 11betaHSD1 are described

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