113269-06-0 Usage
Uses
Used in Pharmaceutical Synthesis:
4-Fluoro-5-nitrobenzene-1,2-diamine serves as a key intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the development of new drugs with potential therapeutic applications, including those targeting specific diseases or conditions.
Used in Agrochemical Production:
4-FLUORO-5-NITROBENZENE-1,2-DIAMINE is also utilized in the production of agrochemicals, contributing to the development of pesticides, herbicides, and other agricultural chemicals that help protect crops and enhance agricultural productivity.
Used in Dye Manufacturing:
4-Fluoro-5-nitrobenzene-1,2-diamine is employed in the manufacturing of dyes, where its chemical properties contribute to the creation of a wide range of colorants used in various industries, such as textiles, plastics, and printing.
Used in Organic Synthesis:
As a building block in organic synthesis, 4-fluoro-5-nitrobenzene-1,2-diamine is instrumental in the creation of complex organic molecules, facilitating the development of new chemical compounds with diverse applications.
Used in Polymer Production:
4-FLUORO-5-NITROBENZENE-1,2-DIAMINE plays a role in the production of polymers, which are essential materials in numerous industries, including plastics, coatings, and adhesives.
Used in Cancer Treatment Research:
4-Fluoro-5-nitrobenzene-1,2-diamine has been studied for its potential applications in cancer treatment, with ongoing research exploring its ability to target and affect cancer cells, offering new possibilities for therapeutic intervention.
Used in Bioactive Compound Synthesis:
As an intermediate in the synthesis of bioactive compounds, 4-fluoro-5-nitrobenzene-1,2-diamine contributes to the development of substances with biological activity, which may have applications in medicine, agriculture, and other fields.
Check Digit Verification of cas no
The CAS Registry Mumber 113269-06-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,2,6 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 113269-06:
(8*1)+(7*1)+(6*3)+(5*2)+(4*6)+(3*9)+(2*0)+(1*6)=100
100 % 10 = 0
So 113269-06-0 is a valid CAS Registry Number.
InChI:InChI=1/C6H6FN3O2/c7-3-1-4(8)5(9)2-6(3)10(11)12/h1-2H,8-9H2
113269-06-0Relevant academic research and scientific papers
Sulfonamide-based compounds as protein tyrosine kinase inhibitors
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Page/Page column 12/16; 8; 16, (2008/06/13)
Various sulfonamide-based compounds are able to selectively inhibit the Src family of tyrosine kinases. These compounds are useful in the treatment of various diseases including hyperproliferative diseases, hematologic diseases, osteoporosis, neurological diseases, autoimmune diseases, allergic/immunological diseases, or viral infections.
THE FOUR 6-HALO-7-NITROQUINOXALINES
Nasielski-Hinkens, Raymonde,Leveque, Pierre,Castelet, Daniel,Nasielski, Jacques
, p. 2433 - 2442 (2007/10/02)
The study of relative nucleofugicities of nitro and halogen in quinoxalines required the synthesis of the four 6-halo-7-nitroquinoxalines 2a-d.The fluoro-, chloro- and bromo-derivatives were made from the commercially available or readily accessible 1,2-diamino-4-halobenzenes, using the nitration of the corresponding p-toluenesulfonamides.This scheme failed in the case of the iodo compound because of extensive nitro-deiodination.The synthesis of 6-iodo-7-nitroquinoxaline was finally achieved from m-fluoroiodobenzene by taking advantage of the high reactivity of fluorine, compared to iodine, in 2,4-dinitrohalobenzenes.
