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Ethanone, 1-[4-[(3-aminophenyl)methoxy]-2-hydroxy-3-propylphenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104013-60-7

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104013-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104013-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,1 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 104013-60:
(8*1)+(7*0)+(6*4)+(5*0)+(4*1)+(3*3)+(2*6)+(1*0)=57
57 % 10 = 7
So 104013-60-7 is a valid CAS Registry Number.

104013-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-[(3-aminophenyl)methoxy]-2-hydroxy-3-propylphenyl]ethanone

1.2 Other means of identification

Product number -
Other names -

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:104013-60-7 SDS

104013-60-7Relevant academic research and scientific papers

POTENTIATORS OF GLUTAMATE RECEPTORS

-

Page/Page column 123, (2010/11/08)

The present invention provides compounds of formula (I); pharmaceutical compositions thereof, and methods of using the same, processes or preparing the same, and intermediates thereof.

Synthesis and Antiallergic Activity of a Novel Series of 5-Lipoxygenase Inhibitors

Kees, Kenneth L.,Musser, John H.,Chang, Joseph,Skowronek, Maureen,Lewis, Alan J.

, p. 2329 - 2334 (2007/10/02)

A series of novel substituted amino>oxoalkanoic acid esters have been synthesized.These compounds were tested in vitro for their ability to inhibit the synthesis of 5-hydroxyeicosatetraenoic acid and leukotriene (LT)B4 f

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