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Benzoic acid, 2-[(2-methoxyphenyl)amino]-5-nitro-, is a complex organic compound with the chemical formula C14H12N2O4. It is a derivative of benzoic acid, featuring a nitro group at the 5-position and an amino group connected to a 2-methoxyphenyl moiety at the 2-position. Benzoic acid, 2-[(2-methoxyphenyl)amino]-5-nitro- is known for its potential applications in the synthesis of pharmaceuticals and other organic compounds. It is characterized by its yellow crystalline appearance and is typically used in a laboratory setting due to its reactivity and the need for controlled conditions. The compound's properties, such as its solubility and stability, are important considerations in its handling and use.

5291-56-5

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5291-56-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5291-56-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,9 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5291-56:
(6*5)+(5*2)+(4*9)+(3*1)+(2*5)+(1*6)=95
95 % 10 = 5
So 5291-56-5 is a valid CAS Registry Number.

5291-56-5SDS

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 2-(2-methoxyanilino)-5-nitrobenzoic acid

1.2 Other means of identification

Product number -
Other names 4-Nitro-2'-methoxydiphenylamin-2-carbonsaeure

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:5291-56-5 SDS

5291-56-5Downstream Products

5291-56-5Relevant academic research and scientific papers

Novel P2Y12 receptor antagonists

-

Page/Page column 37; 53-54, (2008/12/08)

The present invention relates to compounds of Formula I, in which A and B are independently CH2, O, S, NH, C=O, C=NH, C=S or C=N-OH; X is NH, O, S, C=O or CH2 and R1-R5 are as defined in claim 1, which are P2Y12 receptor antagonists and useful for treating, alleviating and/or preventing diseases and disorders related to P2Y12 receptor function as well as pharmaceutical compositions comprising such compounds and methods for preparing such compounds. The present invention is further directed to the use of these compounds, alone or in combination with other therapeutic agents, for the alleviation, prevention and/or treatment of diseases and disorders, especially the use as antithrombotic agents for inhibiting platelet aggregation.

Catalyst-free microwave-assisted amination of 2-chloro-5-nitrobenzoic acid

Baqi, Younis,Mueller, Christa E.

, p. 5908 - 5911 (2008/02/10)

(Chemical Equation Presented) The synthesis of N-substituted 5-nitroanthranilic acid derivatives 3a-w was achieved by a new, mild, microwave-assisted, regioselective amination reaction of 5-nitro-2-chlorobenzoic acid (1a) with a diverse range of aliphatic

Convenient access to substituted acridines by a Buchwald-Hartwig amination

Csuk, René,Barthel, Alexander,Raschke, Christian

, p. 5737 - 5750 (2007/10/03)

A convenient, high yield procedure for the synthesis of anthranilic acids carrying a variety of different substituents as well as their straightforward transformation into the corresponding 9-chloroacridines could be established by using modified Buchwald-Hartwig amination conditions.

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