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15307-77-4

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15307-77-4 Usage

Chemical Properties

Light Tan Solid

Uses

A Diclofenac derivative as anti-inflammatory and analgesic agent.

Check Digit Verification of cas no

The CAS Registry Mumber 15307-77-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,3,0 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 15307-77:
(7*1)+(6*5)+(5*3)+(4*0)+(3*7)+(2*7)+(1*7)=94
94 % 10 = 4
So 15307-77-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H15Cl2NO2/c1-2-21-15(20)10-11-6-3-4-9-14(11)19-16-12(17)7-5-8-13(16)18/h3-9,19H,2,10H2,1H3

15307-77-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-[2-(2,6-dichloroanilino)phenyl]acetate

1.2 Other means of identification

Product number -
Other names ethyl 2-[(2,6-dichlorophenyl)amino]benzeneacetate

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:15307-77-4 SDS

15307-77-4Relevant articles and documents

Design of multifaceted antioxidants: Shifting towards anti-inflammatory and antihyperlipidemic activity

Kourounakis, Angeliki,Lambrinidis, George,Tzara, Ariadni

, (2021/08/30)

Oxidative stress and inflammation are two conditions that coexist in many multifactorial diseases such as atherosclerosis and neurodegeneration. Thus, the design of multifunctional compounds that can concurrently tackle two or more therapeutic targets is an appealing approach. In this study, the basic NSAID structure was fused with the antioxidant moieties 3,5-di-tert-butyl-4-hydroxybenzoic acid (BHB), its reduced alcohol 3,5-di-tert-butyl- 4-hydroxybenzyl alcohol (BHBA), or 6-hydroxy-2,5,7,8-tetramethylchromane-2-carboxylic acid (Trolox), a hydrophilic analogue of α-tocopherol. Machine learning algorithms were utilized to validate the potential dual effect (anti-inflammatory and antioxidant) of the designed analogues. Derivatives 1-17 were synthesized by known esterification methods, with good to excellent yields, and were pharmacologically evaluated both in vitro and in vivo for their antioxidant and anti-inflammatory activity, whereas selected compounds were also tested in an in vivo hyperlipidemia protocol. Furthermore, the activity/binding affinity of the new compounds for lipoxygenase-3 (LOX-3) was studied not only in vitro but also via molecular docking simulations. Experimental results demonstrated that the antioxidant and anti-inflammatory activities of the new fused molecules were increased compared to the parent molecules, while molecular docking simulations validated the improved activity and revealed the binding mode of the most potent inhibitors. The purpose of their design was justified by providing a potentially safer and more efficient therapeutic approach for multifactorial diseases.

Design, synthesis and QSAR studies on a series of 2, 5-disubstituted-1,3,4-oxadiazole derivatives of diclofenac and naproxen for analgesic and anti-inflammatory activity

Ilango, Kaliappan,Valentina, Parthiban,Kumar, Gajendra,Dixit, Dushyant,Nilewar, Shrikant,Kathiravan, Muthu K.

, p. 753 - 763 (2015/12/01)

A series of twenty molecules belonging to 2, 5-disubstituted-1, 3, 4-oxadiazole derivatives of Diclofenac and Naproxen were designed, synthesized and their structures were confirmed by spectroscopy. The target compounds were evaluated for anti-inflammator

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