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Ethanone, 1-[2-hydroxy-4-(1-methylethoxy)phenyl]-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

50561-04-1

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50561-04-1 Usage

Preparation

Obtained by partial alkylation of benzyl 2,4-di-hydroxyphenyl ketone with isopropyl bromide in DMF in the presence of potassium carbonate (79%).

Check Digit Verification of cas no

The CAS Registry Mumber 50561-04-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,5,6 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 50561-04:
(7*5)+(6*0)+(5*5)+(4*6)+(3*1)+(2*0)+(1*4)=91
91 % 10 = 1
So 50561-04-1 is a valid CAS Registry Number.

50561-04-1SDS

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-(2-hydroxy-4-propan-2-yloxyphenyl)-2-phenylethanone

1.2 Other means of identification

Product number -
Other names 2-hydroxy-4-isopropoxy-phenyl-benzyl-ketone

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:50561-04-1 SDS

50561-04-1Relevant academic research and scientific papers

Stability and chemical reactivity of 7-isopropoxyisoflavone (ipriflavone)

Varga, Marton,Batori, Sandor,Koevari-Radkai, Maria,Prohaszka-Nemet, Ildiko,Vitanyi-Morvai, Magdolna,Boecskey, Zsolt,Bokotey, Sandor,Simon, Kalman,Hermecz, Istvan

, p. 3911 - 3920 (2007/10/03)

The stability (hydrolysis and oxidation) of ipriflavone (7-isopropoxyisoflavone, 1) was studied under basic and acidic conditions in different solvents; the effects of irradiation were investigated in methanol. Identification of the isolated products enabled suggestions to be made concerning the mechanisms of decomposition.

Metabolic 5-methyl-isoflavone-derivatives, process for the preparation thereof and compositions containing the same

-

, (2008/06/13)

Nonestrogenic 5-methyl-alkoxy-isoflavone, namely, 5-methyl-7-methoxy-isoflavone, 5-methyl-7-ethoxy-isoflavone, 5-methyl-7-isopropoxy-isoflavone, and 5-methyl-7-(2-hydroxy-ethoxy)-isoflavone are useful as weight-gain promoters in feeds from which the 7-methoxy and 7-ethoxy isoflavones have been excluded because of estrogenic effects. They are more effective than 7-isopropoxy-isoflavone as well.

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