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2-Hydroxy-N-(naphthalen-1-yl)benzamide is a chemical compound with the molecular formula C17H13NO2. It is a derivative of benzamide, featuring a hydroxyl group (-OH) at the 2nd position and a naphthalene ring attached to the nitrogen atom. This organic molecule is known for its potential applications in pharmaceuticals and materials science, particularly in the development of new drugs and as a building block for more complex organic compounds. Its structure provides a foundation for further functionalization and exploration of its chemical properties.

5343-69-1

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5343-69-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5343-69-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,4 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5343-69:
(6*5)+(5*3)+(4*4)+(3*3)+(2*6)+(1*9)=91
91 % 10 = 1
So 5343-69-1 is a valid CAS Registry Number.

5343-69-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-1-NAPHTHYLSALICYLAMIDE

1.2 Other means of identification

Product number -
Other names 3-hydroxy-N-methylsuccinimide

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:5343-69-1 SDS

5343-69-1Downstream Products

5343-69-1Relevant academic research and scientific papers

One-pot synthesis of salicylanilides by direct amide bond formation from salicyclic acid under microwave irradiation

Lu, Cheng-Rong,Zhao, Bei,Jiang, Ying-Peng,Ding, Hao,Yang, Sheng

experimental part, p. 1257 - 1266 (2011/05/07)

A highly efficient protocol for the preparation of aromatic amides is described by the direct reactions between salicyclic acid and aromatic amines in the presence of phosphorous trichloride under microwave irradiation. The method has several advantages over the conventional methods, including operational simplicity, good yield, and reduced reaction time.

BORON TRICHLORIDE CATALYZED ORTHO CARBONYLATION OF PHENOLS: SYNTHESIS OF 2-HYDROXY-ARYL-CARBOXYAMIDES AND -KETONES.

Piccolo, Oreste,Filippini, Lucio,Tinucci, Laura,Valoti, Ermanno,Citterio, Attilio

, p. 885 - 892 (2007/10/02)

In the presence of equimolar quantity of BCl3, phenols 1 react with isocyanates and acyl chlorides to give, usually with good-excellent yields, 2-hydroxy-aryl-carboxy-amides 2 and 2-hydroxy-aryl-ketones 3 respectively.A distinctive behaviour of BCl3 in comparison with other Lewis acids is observed.

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