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2741-55-1

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2741-55-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2741-55-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,4 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2741-55:
(6*2)+(5*7)+(4*4)+(3*1)+(2*5)+(1*5)=81
81 % 10 = 1
So 2741-55-1 is a valid CAS Registry Number.

2741-55-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[4-(2-nitrophenoxy)phenyl]acetamide

1.2 Other means of identification

Product number -
Other names Essigsaeure-[4-(2-nitro-phenoxy)-anilid]

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:2741-55-1 SDS

2741-55-1Relevant articles and documents

2-Carbomethoxy-3-hydroxyquinoxaline-di-N-oxide as a novel ligand for the copper-catalyzed coupling reaction of phenols and aryl halides

Qiu, Yatao,Jia, Weijun,Yao, Zhiyi,Wu, Fanhong,Jiang, Sheng

, p. 1502 - 1510 (2013/05/08)

2-Carbomethoxy-3-hydroxyquinoxaline-di-N-oxide was identified as an efficient novel ligand for the copper-catalyzed coupling of aryl halides with various phenols under mild conditions. The catalytic system shows great functional-group tolerance and excellent reactive selectivity.

Synthesis of 3,4,4′- and 2′,3,4-triaminodiphenyl ethers

Pilyugin,Mikhailyuk,Kiseleva,Kuznetsova,Chikisheva,Kosareva

, p. 1105 - 1109 (2007/10/03)

Procedures were developed for preparing 3,4,4′- and 2′,3,4-triaminodiphenyl ethers by the reaction of 4-acetylaminophenol with, respectively, 4-nitro- or 2-nitrochlorobenzene, followed by nitration of the resulting 4-acetylamino-4′- or -2′-nitrodiphenyl ether, hydrolysis of the product, 4-acetylamino-3,4′- or -2′,3- dinitrodiphenyl ether, and reduction of 4-amino-3,4′- or -2′-3-dinitrodiphenyl ether.

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