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5-AMINO-2-FLUORO-4-NITROBENZOTRIFLUORIDE is a chemical compound characterized by its molecular formula C7H4F4N2O2. It is a yellow solid that serves as a crucial building block in the realm of organic synthesis. 5-AMINO-2-FLUORO-4-NITROBENZOTRIFLUORIDE is distinguished by its potent electron-withdrawing properties, which render it an indispensable reagent in the creation of pharmaceuticals and agrochemicals. Furthermore, it plays a significant role in the synthesis of dyes and pigments. Given its reactivity and potential health risks, the careful handling and storage of 5-AMINO-2-FLUORO-4-NITROBENZOTRIFLUORIDE are of paramount importance.

179062-05-6

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179062-05-6 Usage

Uses

Used in Pharmaceutical Industry:
5-AMINO-2-FLUORO-4-NITROBENZOTRIFLUORIDE is used as a key intermediate in the synthesis of various pharmaceuticals due to its strong electron-withdrawing properties, which facilitate the development of new drug molecules with improved efficacy and safety profiles.
Used in Agrochemical Industry:
In the agrochemical sector, 5-AMINO-2-FLUORO-4-NITROBENZOTRIFLUORIDE is utilized as a building block for the production of agrochemicals, contributing to the development of innovative and effective crop protection agents.
Used in Dye and Pigment Synthesis:
5-AMINO-2-FLUORO-4-NITROBENZOTRIFLUORIDE is employed as a reagent in the synthesis of dyes and pigments, enabling the creation of a wide range of colorants for various applications, including textiles, plastics, and printing inks.
Used in Organic Synthesis:
As a versatile building block in organic synthesis, 5-AMINO-2-FLUORO-4-NITROBENZOTRIFLUORIDE is used for the preparation of a variety of organic compounds, including those with potential applications in materials science, chemical research, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 179062-05-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,0,6 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 179062-05:
(8*1)+(7*7)+(6*9)+(5*0)+(4*6)+(3*2)+(2*0)+(1*5)=146
146 % 10 = 6
So 179062-05-6 is a valid CAS Registry Number.
InChI:InChI=1/C7H4F4N2O2/c8-4-2-6(13(14)15)5(12)1-3(4)7(9,10)11/h1-2H,12H2

179062-05-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H64928)  4-Fluoro-2-nitro-5-(trifluoromethyl)aniline, 98%   

  • 179062-05-6

  • 250mg

  • 294.0CNY

  • Detail
  • Alfa Aesar

  • (H64928)  4-Fluoro-2-nitro-5-(trifluoromethyl)aniline, 98%   

  • 179062-05-6

  • 1g

  • 784.0CNY

  • Detail
  • Alfa Aesar

  • (H64928)  4-Fluoro-2-nitro-5-(trifluoromethyl)aniline, 98%   

  • 179062-05-6

  • 5g

  • 2940.0CNY

  • Detail

179062-05-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluoro-2-nitro-5-(trifluoromethyl)aniline

1.2 Other means of identification

Product number -
Other names 5-Amino-2-fluoro-4-nitrobenzotrifluoride

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:179062-05-6 SDS

179062-05-6Relevant academic research and scientific papers

2-Substituted benzimidazole derivatives as selective melanin concentrating hormone receptor antagonists for the treatment of obesity and related disorders

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Page/Page column 34, (2010/02/11)

The present invention discloses compounds of formula I wherein Ar, X, R1 and R11 are herein defined, said compounds being novel antagonists for melanin-concentrating hormone (MCH), as well as methods for preparing such compounds. In

Glycine receptor antagonists and the use thereof

-

, (2008/06/13)

Methods of treating or preventing neuronal loss associated with stroke, ischemia, CNS trauma, hypoglycemia and surgery, as well as treating neurodegenerative diseases including Alzheimer's disease, amyotrophic lateral sclerosis, Huntington's disease and Down's syndrome, treating or preventing the adverse consequences of the hyperactivity of the excitatory amino acids, as well as treating anxiety, chronic pain, convulsions, inducing anesthesia and treating psychosis are disclosed by administering to an animal in need of such treatment a compound having high affinity for the glycine binding site, lacking PCP side effects and which crosses the blood brain barrier of the animal. Also disclosed are novel 1,4-dihydroquinoxaline-2,3-diones, and pharmaceutical compositions thereof. Also disclosed are highly soluble ammonium salts of 1,4-dihydroquinoxaline-2,3-diones.

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