147285-87-8

Usage

Uses

Used in Pharmaceutical Industry:
2-Amino-5-fluoro-3-nitrotoluene, 2-Amino-5-fluoro-3-methyl-1-nitrobenzene are used as intermediates for the synthesis of pharmaceuticals, contributing to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Amino-5-fluoro-3-nitrotoluene, 2-Amino-5-fluoro-3-methyl-1-nitrobenzene serve as intermediates in the production of agrochemicals, such as pesticides and herbicides, to enhance crop protection and yield.
Used in Dye Industry:
2-Amino-5-fluoro-3-nitrotoluene, 2-Amino-5-fluoro-3-methyl-1-nitrobenzene are utilized as intermediates in the synthesis of dyes, playing a crucial role in the creation of various colorants for different applications, including textiles, plastics, and printing inks.

InChI:InChI=1/C7H7FN2O2/c1-4-2-5(8)3-6(7(4)9)10(11)12/h2-3H,9H2,1H3

Upstream product

• 366-44-9 2-chloro-N-(4-fluoro-2-methylphenyl)acetamide 
• 452-71-1 4-fluor-2-methylaniline 
• 326-65-8 N-(4-fluoro-2-methylphenyl)acetamide 
• 159020-73-2 N-(4-fluoro-2-methyl-6-nitrophenyl)acetamide 
• 446-33-3 5-Fluoro-2-nitrotoluene 

Downstream Products

• 1463053-91-9 2-bromo-5-fluoro-1-methyl-3-nitrobenzene 
• 1463053-93-1 2-bromo-5-fluoro-3-methylaniline 
• 206647-96-3 5-fluoro-3-methyl-1,2-phenylenediamine 

Relevant academic research and scientific papers

FGFR4 INHIBITOR AND PREPARATION METHOD AND USE THEREOF

Provided are a class of compounds as shown in formula (I) as FGFR4 inhibitors, and pharmaceutically acceptable salts thereof, preparation methods therefor and the use thereof in the preparation of drugs for treating FGFR4-related diseases.

Fluorine-containing substituted 7-bromo-benzothiadiazole-4-carboxaldehyde and synthetic method thereof

The invention belongs to the technical field of photoelectric materials, and provides fluorine-containing substituted 7-bromo-benzothiadiazole-4-carboxaldehyde and a synthetic method thereof. The synthetic method comprises the following steps: dropwise ad

CINNOLINE DERIVATIVES AS AS BTK INHIBITORS

Disclosed are compounds of Formula 1, and pharmaceutically acceptable salts thereof, wherein R1, R2, R3, R4, and R5 are defined in the specification. The compounds are inhibitors of Bruton's tyrosine

Insecticidal substituted-2,4-diaminoquinazolines

An insecticidal composition comprising, in admixture with an agriculturally acceptable carrier, an insecticidally effective amount of a 2,4-diaminoquinazoline compound of the formula: STR1 wherein R1, R2, R6, R7, W, X, Y, and Z are as defined herein; methods of using the same; novel 2,4-diaminoquinazolines per se; and intermediates in the preparation thereof.

Nitration of 5-Fluoro-2,1,3-benzoselenadiazoles, and the Synthesis of 4-Fluoro-3-nitro-, 4-Fluoro-6-nitro, 5-Fluoro-3-nitro-o-phenylenediamines and 3,4-Diamino-2-nitrophenols by Subsequent Deselenation

Fuming nitric and concentrated sulfuric acids converted the title benzoselenadiazoles 1 and 8 into their 4- and/or 7-nitro derivatives.Unlike the m-fluoronitro substituted products 6 and 9, the o-fluoronitro substituted products 2 were accompanied by the