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49565-62-0

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49565-62-0 Usage

Derivative of benzoic acid

2-(methylamino)-4-nitrobenzoic acid is derived from benzoic acid, which means it is a modified version of the parent compound benzoic acid.

Methylamino group

This compound contains a methylamino group (-NHCH3) attached to the benzene ring, which contributes to its chemical properties and reactivity.

Nitro group

The presence of a nitro group (-NO2) on the benzene ring makes 2-(methylamino)-4-nitrobenzoic acid more reactive and contributes to its potential applications in the synthesis of various drugs and organic compounds.

Use in pharmaceutical and chemical industries

2-(methylamino)-4-nitrobenzoic acid is commonly used as an intermediate in the synthesis of various drugs and organic compounds, making it an important compound in these industries.

Reagent in organic chemistry

This compound is also used as a reagent for the production of other compounds, showcasing its versatility in chemical reactions.

Potential applications in drug and material development

Due to its unique chemical properties and structure, 2-(methylamino)-4-nitrobenzoic acid has potential applications in the development of new drugs and materials.

Health and environmental hazards

It is important to handle 2-(methylamino)-4-nitrobenzoic acid with care, as it may pose potential health and environmental hazards if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 49565-62-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,5,6 and 5 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 49565-62:
(7*4)+(6*9)+(5*5)+(4*6)+(3*5)+(2*6)+(1*2)=160
160 % 10 = 0
So 49565-62-0 is a valid CAS Registry Number.

49565-62-0Downstream Products

49565-62-0Relevant articles and documents

TROPOMYOSIN RECEPTOR KINASE (TRK) DEGRADATION COMPOUNDS AND METHODS OF USE

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Page/Page column 310, (2021/09/04)

This disclosure relates to bivalent compounds (e.g., bi-functional small molecule compounds), compositions comprising one or more of the bivalent compounds, and to methods of use the bivalent compounds for the treatment of certain disease in a subject in need thereof. The disclosure also relates to methods for identifying such bivalent compounds.

CRBN LIGANDS AND USES THEREOF

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Paragraph 00327-00328, (2019/04/16)

The present invention provides compounds, compositions thereof, and methods of using the same for the inhibition of CRBN, and the treatment of CRBN-mediated disorders.

Efficient copper-catalyzed synthesis of N-alkylanthranilic acids via an ortho-substituent effect of the carboxyl group of 2-halobenzoic acids at room temperature

Zeng, Liang,Fu, Hua,Qiao, Renzhong,Jiang, Yuyang,Zhao, Yufen

supporting information; experimental part, p. 1671 - 1676 (2011/02/25)

We have developed an efficient copper-catalyzed method for the synthesis of N-alkylanthranilic acids. The protocol uses inexpensive copper(I) iodide/racemic 1,1'-binaphthyl-2,2'-diol (rac-BINOL) as the catalyst/ligand system, readily available 2-halobenzoic acids and aliphatic amines as the starting materials, the coupling reactions were performed at room temperature, and various functionalities in the substrates were tolerated.

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