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Ethanone, 1-(3-fluoro-4-methoxyphenyl)-2-phenyl-, also known as 1-(3-fluoro-4-methoxyphenyl)-2-phenylethanone, is an organic compound with the molecular formula C15H13FO2. It is a derivative of acetophenone, featuring a fluorine atom at the 3-position and a methoxy group at the 4-position of the phenyl ring attached to the carbonyl group. Ethanone, 1-(3-fluoro-4-methoxyphenyl)-2-phenyl- is characterized by its unique structure, which combines the properties of a ketone with the electronic effects of a fluorine atom and a methoxy group. It is used in the synthesis of various pharmaceuticals and agrochemicals due to its potential to modulate the activity of the final products through its electron-withdrawing and electron-donating properties. The compound's specific structure and functional groups make it a valuable intermediate in the development of new molecules with desired biological activities.

325-62-2

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325-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 325-62-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 325-62:
(5*3)+(4*2)+(3*5)+(2*6)+(1*2)=52
52 % 10 = 2
So 325-62-2 is a valid CAS Registry Number.

325-62-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(3-fluoro-4-methoxyphenyl)-2-phenyl-ethan-1-one

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:325-62-2 SDS

325-62-2Relevant academic research and scientific papers

ESTROGEN MODULATORS

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Page/Page column 37, (2008/06/13)

The present application is directed to a new class of isoxazoles and their use as estrogen modulators.

Substituted isoxazoles for the treatment of inflammation

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Page 24-25; 57, (2010/11/30)

A class of substituted isoxazolyl compounds is described for use in treating inflammation and inflammation-related disorders. Compounds of particular interest are defined by Formula (III) wherein R7 is selected from hydroxyl, lower alkyl, carboxyl, halo, lower carboxylalkyl, lower alkoxycarbonylalkyl, lower alkoxyalkyl, lower carboxyalkoxyalkyl, lower haloalkyl, lower haloalkylsulfonyloxy, lower hydroxyalkyl, lower aryl (hydroxylalkyl), lower carboxyaryloxyalkyl, lower alkoxycarbonylaryloxyalkyl, lower cycloalkyl, lower cycloalkylalkyl, and lower aralkyl; and wherein R8 is one or more radicals independently selected from hydrido, lower alkylsulfinyl, lower alkyl, cyano, carboxyl, lower alkoxycarbonyl, lower haloalkyl, hydroxyl, lower hydroxyalkyl, lower haloalkoxy, amino, lower alkylamino, lower arylamino, lower aminoalkyl, nitro, halo, lower alkoxy, aminosulfonyl, and lower alkylthio; or a pharmaceutically-acceptable salt thereof.

Isoxazole compounds as cyclooxygenase inhibitors

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, (2008/06/13)

A class of substituted isoxazolyl compounds is described for use in treating cyclooxygenase-2 related disorders. Compounds of particular interest are defined by Formula I STR1 wherein R1, R2, and R3, are described in the specification.

Synthesis and activity of sulfonamide-substituted 4,5-diaryl thiazoles as selective cyclooxygenase-2 inhibitors

Carter, Jeffery S.,Kramer, Steven,Talley, John J.,Penning, Thomas,Collins, Paul,Graneto, Matthew J.,Seibert, Karen,Koboldt, Carol M.,Masferrer, Jaime,Zweifel, Ben

, p. 1171 - 1174 (2007/10/03)

A series of sulfonamide-substituted 4,5-diarylthiazoles was prepared via three synthetic routes as selective COX-2 inhibitors. Recently in the synthesis of selective COX-2 inhibitors we have discovered that the sulfonamide moiety is a suitable replacement

SUBSTITUTED ISOXAZOLES FOR THE TREATMENT OF INFLAMMATION

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, (2008/06/13)

A class of substituted isoxazolyl compounds is described for use in treating inflammation and inflammation-related disorders. Compounds of particular interest are defined by Formula II wherein R1 is selected from hydroxyl, lower alkyl, carboxyl, lower carboxyalkyl, lower aminocarbonylalkyl, lower alkoxycarbonylalkyl, lower aralkyl, lower alkoxyalkyl, lower aralkoxyalkyl, lower alkylthioalkyl, lower aralkylthioalkyl, lower alkylaminoalkyl, lower aryloxyalkyl, lower arylthioalkyl, lower haloalkyl, lower hydroxylalkyl, cycloalkyl, cycloalkylalkyl, and aralkyl; wherein R3 is selected from cycloalkyl, cycloalkenyl, aryl, and heteroaryl; wherein R3 is optionally substituted at a substitutable position with one or more radicals independently selected from lower alkylsulfinyl, lower alkyl, cyano, carboxyl, lower alkoxycarbonyl, lower haloalkyl, hydroxyl, lower hydroxyalkyl, lower haloalkoxy, amino, lower alkylamino, lower arylamino, lower aminoalkyl, nitro, halo, lower alkoxy, aminosulfonyl, and lower alkylthio; and wherein R4 is selected from lower alkyl, hydroxyl and amino; or a pharmaceutically-acceptable salt thereof

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