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Benzamide, 3-fluoro-N-(4-methylphenyl)-, also known as 3-fluoro-4'-methyl-N-phenylbenzamide, is a chemical compound with the molecular formula C14H12FNO and a molecular weight of 227.25 g/mol. It is a white to off-white crystalline solid that is soluble in organic solvents such as ethanol, methanol, and acetonitrile. Benzamide, 3-fluoro-N-(4-methylphenyl)- is primarily used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the development of new drugs targeting the central nervous system. Its unique structure, featuring a fluorine atom and a methyl group on the phenyl ring, contributes to its potential applications in medicinal chemistry, as these functional groups can influence the compound's biological activity and pharmacokinetic properties.

398-80-1

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398-80-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 398-80-1 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,9 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 398-80:
(5*3)+(4*9)+(3*8)+(2*8)+(1*0)=91
91 % 10 = 1
So 398-80-1 is a valid CAS Registry Number.

398-80-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-fluoro-N-(4-methylphenyl)benzamide

1.2 Other means of identification

Product number -
Other names 3-fluoro-benzoic acid p-toluidide

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:398-80-1 SDS

398-80-1Downstream Products

398-80-1Relevant academic research and scientific papers

Ligand-free copper-catalyzed direct amidation of diaryliodonium salts using nitriles as amidation reagents

Cheng, Hui-cheng,Guo, Penghu,Ji, Hong-bing,Ma, Jiao-li,Zhang, Yang,Zhou, Lichao,Zhou, Xuming

, (2021)

An efficient and practical methodology for the synthesis of N-arylamides has been developed via copper-catalyzed amidation of diaryliodonium salts with nitriles. Various substituted aryl nitriles and aliphatic nitriles could be applied in the reaction, providing a series of N-arylated amides in moderate to good yields. This procedure provides an alternative route for the synthesis of various N-arylamides. A proposed mechanism based on control experiments is also presented.

Preparation method of N-aryl amide compound

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Paragraph 0072-0076, (2020/07/13)

The invention discloses a preparation method of an N-aryl amide compound, which comprises the following steps: (1) putting diaryliodonium salt and Cu(OAc)2 into a Schlenk tube provided with a magneticstirring rod; (2) sequentially adding DCE, H2O and nitrile by using an injector, sealing the Schlenk tube, and stirring for reaction at 80 DEG C; (3) cooling the obtained solution to room temperature, and performing extraction with EtOAc; and combining organic layers, performing washing with saline water, and performing drying with anhydrous Na2SO4; and (4) removing volatile matters in vacuum, and purifying residues through column chromatography to obtain the N-aryl amide compound. Through a large number of experiments, a substrate with a simple structure is screened, the reaction conditionsare mild, the yield is high, the pollution is small, and the application prospect is wide.

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