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4-[(4-chlorobenzyl)oxy]-N-(3,4-dichlorophenyl)-3-methoxybenzamide is a complex organic compound with the molecular formula C21H17Cl3NO3. It is a derivative of benzamide, featuring a 4-chlorobenzyloxy group attached to the 4-position, a 3,4-dichlorophenyl group at the amide nitrogen, and a methoxy group at the 3-position. This chemical is known for its potential applications in pharmaceuticals, particularly as an inhibitor of cyclooxygenase enzymes, which are involved in the production of prostaglandins and can be targeted for the treatment of inflammation and pain. The compound's structure and properties make it a subject of interest in medicinal chemistry and drug development.

6407-12-1

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6407-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6407-12-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,4,0 and 7 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6407-12:
(6*6)+(5*4)+(4*0)+(3*7)+(2*1)+(1*2)=81
81 % 10 = 1
So 6407-12-1 is a valid CAS Registry Number.

6407-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[(4-chlorophenyl)methoxy]-N-(3,4-dichlorophenyl)-3-methoxybenzamide

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

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More Details:6407-12-1 SDS

6407-12-1Upstream product

6407-12-1Downstream Products

6407-12-1Relevant academic research and scientific papers

15N NUCLEAR POLARISATION IN NITRATION AND RELATED REACTIONS. PART 2. p-NITROPHENOL

Clemens, Anthony H.,Ridd, John H.,Sandall, John P. B.

, p. 1667 - 1672 (1984)

The nitrous acid-catalysed nitration of p-nitrophenol by H(15)NO3 in aqueous trifluoroacetic acid gives a strong emission signal during reaction for the 2-(15)NO2 group in the 15N n.m.r. spectrum of the 2,4-dinitrophenol formed: the enhancement is by a factor of up to 600.The reaction is accompanied by 11percent migration of the original 4-nitro group to the 2-position and substitution by the labelled nitro group at the 4-position.The 15N n.m.r. spectrum during the related reaction using 15N labelled p-nitrophenol and unlabelled nitric acid shows that the migration of the 4-(15)NO2 group to the 2-position causes a strongly enhanced absorption signal for the 2-(15)NO2 group in the 2,4-dinitrophenol formed.A strongly enhanced absorption signal for this group is also found for the reaction of p-nitrophenol with H(15)NO3 in the presence of sodium azide.The complete set of results is interpreted in terms of nuclear polarisation deriving from the reactions of the radical pair ArO.NO2. when formed either by diffusion or from a singlet precursor.The reaction between hydrazoic acid and nitric acid is catalysed by p-nitrophenol.

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