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2-(2-chlorophenoxy)-N-(pyridin-3-yl)acetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25288-47-5

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25288-47-5 Usage

Chemical composition

Consists of a chlorophenoxy group, a pyridin-3-yl group, and an acetamide group.

Common uses

Used as an herbicide and pesticide to inhibit the growth of unwanted plants and pests.

Activity spectrum

Has broad-spectrum activity against a variety of plant species and can be found in various agricultural products.

Research applications

Has been used in studies to investigate its effects on plant physiology and biochemistry, as well as its potential environmental impact.

Precautions

May pose risks to human health and the environment, so it should be handled with caution.

Check Digit Verification of cas no

The CAS Registry Mumber 25288-47-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,8 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 25288-47:
(7*2)+(6*5)+(5*2)+(4*8)+(3*8)+(2*4)+(1*7)=125
125 % 10 = 5
So 25288-47-5 is a valid CAS Registry Number.

25288-47-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(2-chlorophenoxy)-N-pyridin-3-ylacetamide

1.2 Other means of identification

Product number -
Other names HMS2685A23

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:25288-47-5 SDS

25288-47-5Relevant academic research and scientific papers

Discovery of 2-phenoxyacetamides as inhibitors of the Wnt-depalmitoleating enzyme NOTUM from an X-ray fragment screen

Atkinson, Benjamin N.,Steadman, David,Zhao, Yuguang,Sipthorp, James,Vecchia, Luca,Ruza, Reinis R.,Jeganathan, Fiona,Lines, Georgie,Frew, Sarah,Monaghan, Amy,Kj?r, Svend,Bictash, Magda,Jones, E. Yvonne,Fish, Paul V.

supporting information, p. 1361 - 1369 (2019/08/21)

NOTUM is a carboxylesterase that has been shown to act by mediating the O-depalmitoleoylation of Wnt proteins resulting in suppression of Wnt signaling. Here, we describe the development of NOTUM inhibitors that restore Wnt signaling for use in in vitro disease models where NOTUM over activity is an underlying cause. A crystallographic fragment screen with NOTUM identified 2-phenoxyacetamide 3 as binding in the palmitoleate pocket with modest inhibition activity (IC50 33 μM). Optimization of hit 3 by SAR studies guided by SBDD identified indazole 38 (IC50 0.032 μM) and isoquinoline 45 (IC50 0.085 μM) as potent inhibitors of NOTUM. The binding of 45 to NOTUM was rationalized through an X-ray co-crystal structure determination which showed a flipped binding orientation compared to 3. However, it was not possible to combine NOTUM inhibition activity with metabolic stability as the majority of the compounds tested were rapidly metabolized in an NADPH-independent manner.

Synthesis of N-Azaaryl anilines: An efficient protocol via smiles rearrangement

Xia, Shuai,Wang, Li-Ying,Sun, Heng-Zhi,Yue, Huan,Wang, Xiu-Hua,Tan, Jia-Lian,Wang, Yin,Hou, Di,He, Xiao-Yan,Mun, Ki-Cheol,Kumar, B. Prem,Zuo, Hua,Shin, Dong-Soo

supporting information, p. 394 - 398 (2013/08/25)

An efficient process for the synthesis of N-azaaryl anilines via Smiles rearrangement as a tool. A variety of Nazaaryl anilines were generated by the reaction of substituted phenols, substituted anilines, aminopyridines and chloroacetyl chloride or pyrido

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