28673-36-1 Usage
Uses
Used in Pharmaceutical Industry:
2-METHYL-4-NITROQUINOLINE is used as a building block for the synthesis of various pharmaceuticals, leveraging its diverse biological activities such as antibacterial, antifungal, antiviral, antiparasitic, and anticancer properties. Its presence in these compounds contributes to the development of effective treatments for a wide range of diseases and conditions.
Used in Agrochemical Industry:
In the agrochemical industry, 2-METHYL-4-NITROQUINOLINE is utilized as a building block for the synthesis of agrochemicals, taking advantage of its antimicrobial and antiparasitic properties. This helps in the development of products that protect crops from various pests and diseases, ensuring increased agricultural productivity.
Used in Dye Manufacturing:
2-METHYL-4-NITROQUINOLINE is used as an intermediate in the manufacturing of dyes, contributing to the production of a variety of colorants used in different industries, such as textiles, plastics, and printing inks.
Used in Organic Compounds Synthesis:
As an intermediate, 2-METHYL-4-NITROQUINOLINE is also used in the synthesis of other organic compounds, expanding its applications in various chemical and industrial processes.
Check Digit Verification of cas no
The CAS Registry Mumber 28673-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,6,7 and 3 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28673-36:
(7*2)+(6*8)+(5*6)+(4*7)+(3*3)+(2*3)+(1*6)=141
141 % 10 = 1
So 28673-36-1 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O2/c1-7-6-10(12(13)14)8-4-2-3-5-9(8)11-7/h2-6H,1H3
28673-36-1Relevant academic research and scientific papers
Synthesis method of 4-aminoquinaldine
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Paragraph 0057; 0069; 0070; 0071, (2018/09/08)
The invention relates to a synthesis method of 4-aminoquinaldine. The invention discloses the synthesis method of the 4-aminoquinaldine; the method comprises the following steps: enabling 2-methyl quinoline, taken as a starting raw material, to be subjected to a hydrogen peroxide oxidation reaction in acetic acid so as to generate 2-methylquinoline N-oxide; then, carrying out a nitration reactionto generate 2-methyl-4-nitroquinoline N-oxide; after that, illuminating for carrying out a reaction to generate 2-methyl-4-nitroquinoline; producing 2-methyl-4-aminoquinoline N-oxide by means of interaction of ferric trichloride hexahydrate and hydrazine hydrate in ethanol; finally, carrying out a reduction reaction by using iron powder under the action of acetic acid so as to generate the 4-aminoquinaldine. The synthesis method provided by the invention has the beneficial effects that the used raw materials and reagents are low in price and easy to obtain, the synthesis method is simple and feasible, the reaction conditions are mild, and a simple and convenient synthetic route is opened up to the synthesis of the 4-aminoquinaldine.
An unusual de-nitro reduction of 2-substituted-4-nitroquinolines
Zhou, Yu,Li, Jian,Liu, Hong,Zhao, Linxiang,Jiang, Hualiang
, p. 8511 - 8514 (2007/10/03)
The treatment of a variety of 2-substituted-4-nitroquinolines with Sn in the presence of concentrated hydrochloric acid in ethanol at 70 °C for 2-4 h afforded unusual de-nitro products 2-substituted-quinolines in good yields.
