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4-Chloro-N-(2-Methoxyphenyl)benzaMide, 97% is an organic chemical compound with a purity of 97%. It features a benzene ring with a chlorine atom and a methoxy group attached to it, making it a valuable building block in the synthesis of pharmaceuticals and agrochemicals.
Used in Pharmaceutical Industry:
4-Chloro-N-(2-Methoxyphenyl)benzaMide, 97% is used as an intermediate in the manufacturing of various drugs. Its unique structure allows it to be a key component in the development of new medications, contributing to the advancement of healthcare.
Used in Agrochemical Industry:
In the agrochemical sector, 4-Chloro-N-(2-Methoxyphenyl)benzaMide, 97% serves as an intermediate for the production of pesticides and other agricultural chemicals. Its role in this industry is crucial for creating effective solutions to protect crops and ensure a stable food supply.
Used in Research and Development:
4-Chloro-N-(2-Methoxyphenyl)benzaMide, 97% is also utilized in research and development settings. It is an essential compound for scientists and researchers working on the synthesis of new organic compounds and exploring the potential applications of this chemical in various fields.
It is important to handle 4-Chloro-N-(2-Methoxyphenyl)benzaMide, 97% with care and follow proper safety protocols due to its potential hazards, ensuring the safety of individuals and the environment.

7508-80-7

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7508-80-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7508-80-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,0 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7508-80:
(6*7)+(5*5)+(4*0)+(3*8)+(2*8)+(1*0)=107
107 % 10 = 7
So 7508-80-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H12ClNO2/c1-18-13-5-3-2-4-12(13)16-14(17)10-6-8-11(15)9-7-10/h2-9H,1H3,(H,16,17)

7508-80-7SDS

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 4-chloro-N-(2-methoxyphenyl)benzamide

1.2 Other means of identification

Product number -
Other names 4,2'-Chlormethoxybenzanilid

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:7508-80-7 SDS

7508-80-7Downstream Products

7508-80-7Relevant academic research and scientific papers

Discovery, Optimization, and Biological Evaluation of Sulfonamidoacetamides as an Inducer of Axon Regeneration

Ku, Jin-Mo,Park, Kyuhee,Lee, Jung Hun,Cho, Kyong Jin,Nam, Yeon-Ju,Jeong, Dae-Youn,Kim, Yu-Han,Kwon, Soonjung,Park, Ju-Young,Yang, Jungeun,Nam, Tae-Gyu,Yoon, Sung-Hwa,Ahn, Sangmee,Choi, Yongmun

, p. 4676 - 4687 (2016/06/13)

Axon regeneration after injury in the central nervous system is hampered in part because if an age-dependent decline in the intrinsic axon growth potential, and one of the strategies to stimulate axon growth in injured neurons involves pharmacological manipulation of implicated signaling pathways. Here we report phenotypic cell-based screen of chemical libraries and structure-activity-guided optimization that resulted in the identification of compound 7p which promotes neurite outgrowth of cultured primary neurons derived from the hippocampus, cerebral cortex, and retina. In an animal model of optic nerve injury, compound 7p was shown to induce growth of GAP-43 positive axons, indicating that the in vitro neurite outgrowth activity of compound 7p translates into stimulation of axon regeneration in vivo. Further optimization of compound 7p and elucidation of the mechanisms by which it elicits axon regeneration in vivo will provide a rational basis for future efforts to enhance treatment strategies.

Iron-catalyzed N-arylations of amides

Correa, Arkaitz,Elmore, Simon,Bolm, Carsten

experimental part, p. 3527 - 3529 (2009/04/11)

A method was proposed for iron-catalyzed N-arylation of primary amides and its applicability to the synthesis of N-heterocycles by intramolecular ring closures. The method used a catalyst system of 10 mol % of FeCl3 and 20 mol % of N,N'-dimethylethylenediamine (DMEDA). The study found that secondary amides of N-methylbenzamide and N-benzylbenzamide produce N-arylated products in trace amounts. The method developed an iron-based catalyst system for efficient N-arylations of primary amides with aryl iodides. The study used a sealable tube equipped with a magnetic stir bar charged with amide, or K 3PO4, or K2CO3, or FeCl3. The study used NMR spectroscopic analysis to determine the identity and purity of the products. The method observed that different substituted aryl iodides made a positive impact on the reaction.

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