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3-Amino-5-methoxy-2-nitrobenzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

193481-76-4

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193481-76-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 193481-76-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,3,4,8 and 1 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 193481-76:
(8*1)+(7*9)+(6*3)+(5*4)+(4*8)+(3*1)+(2*7)+(1*6)=164
164 % 10 = 4
So 193481-76-4 is a valid CAS Registry Number.

193481-76-4Relevant academic research and scientific papers

BENZIMIDAZOLES AND RELATED ANALOGS AS SIRTUIN MODULATORS

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Page/Page column 105-106, (2010/04/03)

Provided herein are sirtuin-modulating compounds of formula (II) The sirtuin-modulating compounds may be used for increasing the lifespan of a cell, and treating and/or preventing a wide variety of diseases and disorders including, for example, diseases or disorders related to aging or stress, diabetes, obesity, neurodegenerative diseases, cardiovascular disease, blood clotting disorders, inflammation, cancer, and/or flushing as well as diseases or disorders that would benefit from increased mitochondrial activity. Also provided are compositions comprising a sirtuin-modulating compound in combination with another therapeutic agent.

ORGANIC COMPOUNDS

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Page/Page column 28, (2008/06/13)

Compounds of formula (I) in free or salt form, where Y, R1, R2, R3, R4 and R5 have the meanings as indicated in the specification, are useful for treating conditions that are mediated by the CXCR2 receptor. Pharmaceutical compositions that contain the compounds and a process for preparing the compounds are also described.

A convenient copper-catalyzed direct animation of nitroarenes with 9-alkylhydroxylamines

Seko, Shinzo,Miyake, Kunihito,Kavvamura, Norio

, p. 1437 - 1444 (2007/10/03)

O-Alkylhydroxylamines, particularly O-methylhydroxylamine, aminate nitroarenes in the presence of a strong base and a copper catalyst to give aminonitroarenes in good yields, ortho- or para-Animation with respect to the nitro group takes place, and in some cases the ortho-aminated product is preferentially obtained. With 3-substituted nitrobenzenes where the substituent has a lone pair of electrons, preferential amination occurs at the 2-position to give the sterically most congested 3c-f, 14 and 22g.

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