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102587-44-0

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102587-44-0 Usage

General Description

N-(3,4-dichlorophenyl)-4-methoxybenzamide is a chemical compound with the molecular formula C14H11Cl2NO2. It is a white to off-white solid that is used in various research applications. N-(3,4-dichlorophenyl)-4-methoxybenzamide is a derivative of benzamide, with the addition of a 3,4-dichlorophenyl group and a 4-methoxy group. It is commonly used as a reagent in organic synthesis and medicinal chemistry research. Additionally, it has been studied for its potential pharmacological properties and biological activity, particularly in the context of anti-cancer and anti-inflammatory effects.

Check Digit Verification of cas no

The CAS Registry Mumber 102587-44-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,5,8 and 7 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 102587-44:
(8*1)+(7*0)+(6*2)+(5*5)+(4*8)+(3*7)+(2*4)+(1*4)=110
110 % 10 = 0
So 102587-44-0 is a valid CAS Registry Number.

102587-44-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(3,4-Dichlorophenyl)-4-(hydroxymethyl)benzamide

1.2 Other means of identification

Product number -
Other names 3,4-dichloro-4'-fluorobenzophenone

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:102587-44-0 SDS

102587-44-0Relevant articles and documents

Structure-Activity Studies on Amides Inhibiting Photosystem II

Lewis, Richard J.,Camilleri, Patrick,Kirby, Anthony J.,Marby, Craig A.,Slawin, Alexandra A.,Williams, David J.

, p. 1625 - 1630 (2007/10/02)

A series of N-phenylanilides and N-phenylureas have been synthesised and their 'in vitro' photosystem II activity measured in a cell-free system.An attempt was made to correlate 'in vitro' data with a novel hydrophobicity parameter ?amide (related to the substituent on the phenyl ring) and with the torsion angle θ between the planes of the phenyl and amide moieties.

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