1542-36-5

Usage

Uses

Used in Organic Synthesis:
2,5-Difluoro-4-Nitroaniline is used as a key intermediate in organic synthesis for the production of various compounds. Its unique structure and reactivity make it a valuable building block in the synthesis of complex organic molecules.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2,5-Difluoro-4-Nitroaniline is used as an intermediate in the synthesis of various drugs. Its presence in the molecular structure can impart specific biological activities, contributing to the development of new therapeutic agents.
Used in Dye Industry:
2,5-Difluoro-4-Nitroaniline is used as a precursor in the production of dyes. Its chemical properties allow for the creation of dyes with specific color characteristics and properties, making it an important component in the dye manufacturing process.
Used in Agricultural Chemicals:
In the agricultural sector, 2,5-Difluoro-4-Nitroaniline is used as an intermediate in the synthesis of various agrochemicals, such as pesticides and herbicides. Its unique structure and reactivity contribute to the development of effective and targeted agricultural products.
Used in Material Science:
2,5-Difluoro-4-Nitroaniline has potential applications in material science due to its unique chemical properties. It can be used in the development of new materials with specific characteristics, such as improved stability or reactivity.
Safety Precautions:
It is important to handle 2,5-Difluoro-4-Nitroaniline with care, as it is considered harmful if ingested or inhaled and may cause skin and eye irritation. Proper safety measures, such as wearing protective clothing and using appropriate containment, should be taken during its use and handling.

InChI:InChI=1/C6H4F2N2O2/c7-3-2-6(10(11)12)4(8)1-5(3)9/h1-2H,9H2

Upstream product

• 2105-61-5 1,2,4-trifluoro-5-nitrobenzene 
• 367-30-6 2,5-difluoroaniline 
• 366-53-0 N-(2,5-difluoro-4-nitrophenyl)-acetamide 
• 398-90-3 (2,5-difluorophenyl)acetanilide 
• 404-01-3 N-(3,5-difluorophenyl)acetamide 

Downstream Products

• 195614-50-7 N-ethoxycarbonyl-2,5-difluoro-4-nitroaniline 
• 133531-68-7 1,4-difluoro-2,5-dinitrobenzene 
• 1454650-57-7 4-fluoro-2,5-dinitro-N-propylbenzeneamine 
• 1454650-59-9 4-fluoro-2,5-dinitro-N-propyl-N-trifluoroacetylbenzeneamine 
• 1454650-60-2 N-2,5-dinitro-4-butylaminophenyl-N-propyl-2,2,2-trifluoroacetamide 
• 1454650-61-3 2-butylamino-5-propylamino-1,4-dinitrobenzene 
• 1454650-56-6 1,4-diamino-2-butylamino-5-propylamino benzene 
• 109023-77-0 2-N-methylamino-4-amino-5-fluoronitrobenzene 
• 366-53-0 N-(2,5-difluoro-4-nitrophenyl)-acetamide 
• 4247-61-4 2,5-Difluor-N,N'-diformyl-p-phenylendiamin 
• 578-28-9 1-Chloro-2,5-difluoro-4-nitrobenzene 
• 698-52-2 1,4-diamino-2,5-difluorobenzene 
• 400-05-5 1,4-dichloro-2,5-difluoro-benzene 
• 1454650-58-8 N-5-dipropyl-4-fluoro-2-nitrobenzenediamine 

Relevant academic research and scientific papers

COLLECTIONS OF PEPTIDES, PEPTIDE AGENTS, AND METHODS OF USE THEREOF

The present disclosure provides powerful technologies for the development, production, characterization, and/or use of stapled peptide compositions. Among other things, the present disclosure provides strategies for defining amino acid sequences particularly amenable or useful for stapling, as well as technologies, reagents, and systems for developing, producing, characterizing, and/or using stapled peptides having such amino acid sequences.

2,5-DISUBSTITUTED-1,4-DIAMINOBENZENES

Asymmetrical 2,5-disubstituted-1,4-diaminobenzenes are provided, along with a process for forming both symmetrical and asymmetrical 2,5-disubstituted-1,4-diaminobenzenes.

Herbicidal 3-(bicyclic nitrogen-containing heterocycle)-substituted-1-methyl-6-trifluoromethyluracils

Herbicidal 3-(bicyclic nitrogen-containing heterocycle)-substituted-1-methyl-6-trifluoromethyluracils, compositions containing them, and methods of using them to control undesired plant growth are disclosed. The herbicidal compounds of the present invention are defined by the following generic structure: STR1 in which V is N or C--R1 ; R is hydrogen, straight or branched chain alkyl, alkenyl, alkynyl, hydroxyalkyl, alkoxyalkyl, haloalkyl, alkoxycarbonylalkyl, arylalkyl, optionally substituted with halogen, or aminocarbonylalkyl in which the amino nitrogen is substituted with arylalkyl or one or two alkyl; R1 is hydrogen, alkyl, haloalkyl, or cyano; R2 is lower alkyl or amino; and X is hydrogen or halogen, with the proviso that each aliphatic component has not more than six carbon atoms.

Herbicidal substituted-phenyl-1,2,4-triazol-5(1H)-thiones and -ones

The present application discloses herbicidal substituted-phenyl-1,2,4-Triazole-5(1H)-thiones and -ones, herbicidal compositions containing these compounds, methods of preparing them, and methods for controlling undesired plant growth by preemrgence and/or