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2627-77-2

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2627-77-2 Usage

General Description

4’-Bromosalicylanilide is a chemical compound that is commonly used as an intermediate in the synthesis of pharmaceuticals and dyes. It is an organic compound with the molecular formula C13H10BrNO2 and a molecular weight of 288.13 g/mol. 4'-BROMOSALICYLANILIDE contains a bromine atom, a salicyl group, and an anilide group, and is often utilized as a building block in the manufacturing of various drugs and pigments. In addition, 4’-Bromosalicylanilide has been studied for its potential biological activities, including its anti-inflammatory and antimicrobial properties, making it a valuable compound in the field of medicinal chemistry. Overall, this chemical is a versatile component in the production of various pharmaceutical and industrial products.

Check Digit Verification of cas no

The CAS Registry Mumber 2627-77-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,6,2 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2627-77:
(6*2)+(5*6)+(4*2)+(3*7)+(2*7)+(1*7)=92
92 % 10 = 2
So 2627-77-2 is a valid CAS Registry Number.

2627-77-2SDS

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 N-(4-bromophenyl)-2-hydroxybenzamide

1.2 Other means of identification

Product number -
Other names N-Salicyloyl-4-brom-anilin

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:2627-77-2 SDS

2627-77-2Relevant articles and documents

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.

Potential salicylamide antiplaque agents: In vitro antibacterial activity against Actinomyces viscosus

Coburn,Batista,Evans,Genco

, p. 1245 - 1249 (2007/10/02)

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Studies on 2-hydroxythiobenzamide and 2-hydroxythiobenzanilide. 1. Synthesis of the compounds

Wagner,Singer,Weuffen

, p. 161 - 166 (2007/10/04)

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