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3,4-Bis-trifluoromethyl-phenylamine is an aromatic amine derivative with the molecular formula C8H6F6N. It is characterized by the presence of two trifluoromethyl groups attached to the phenyl ring, which gives it unique chemical properties and potential applications in various fields.

2965-07-3

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2965-07-3 Usage

Uses

Used in Pharmaceutical Industry:
3,4-Bis-trifluoromethyl-phenylamine is used as a building block in organic synthesis for the development of pharmaceuticals. Its unique structure and properties make it a valuable component in the creation of new drugs with potential therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical industry, 3,4-Bis-trifluoromethyl-phenylamine is utilized as a key intermediate in the synthesis of various agrochemicals, such as pesticides and herbicides. Its presence in these compounds can enhance their effectiveness and selectivity in controlling pests and weeds.
Used in Material Science:
3,4-Bis-trifluoromethyl-phenylamine has been studied for its potential applications in material science. Its unique properties may contribute to the development of new materials with improved characteristics, such as enhanced stability, reactivity, or selectivity.
Used as a Reagent in Chemical Reactions:
3,4-Bis-trifluoromethyl-phenylamine also serves as a reagent in various chemical reactions, facilitating the synthesis of complex organic molecules. Its presence can improve the efficiency and selectivity of these reactions, leading to the production of desired products with higher yields.
However, it is crucial to handle 3,4-Bis-trifluoromethyl-phenylamine with caution due to its potential hazards. It can cause irritation and harm if it comes into contact with the skin, eyes, or if inhaled. Therefore, proper safety measures and handling procedures should be followed when working with 3,4-Bis-trifluoromethyl-phenylamine to ensure the safety of individuals and the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 2965-07-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,6 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 2965-07:
(6*2)+(5*9)+(4*6)+(3*5)+(2*0)+(1*7)=103
103 % 10 = 3
So 2965-07-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H5F6NO2/c9-7(10,11)16-5-2-1-4(15)3-6(5)17-8(12,13)14/h1-3H,15H2

2965-07-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,4-bis(trifluoromethyl)aniline

1.2 Other means of identification

Product number -
Other names 3,4-bis-trifluoromethylaniline

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:2965-07-3 SDS

2965-07-3Relevant academic research and scientific papers

Discovery of Potent Antiallergic Agents Based on ano-Aminopyridinyl Alkynyl Scaffold

Bai, Fang,Chen, Taiwen,Fan, Chen,Hu, Youhong,Li, Xin,Liu, Moting,Ma, Yanjie,Tang, Wei,Xiang, Caigui,Xie, Zhicheng

supporting information, p. 13588 - 13603 (2021/09/20)

Effective therapeutic agents are highly desired for immune-mediated allergic diseases. Herein, we report the design, synthesis, and structure-activity relationship of ano-aminopyridinyl alkyne series as novel orally bioavailable antiallergic agents, which

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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