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2,5-Bis(trifluoromethyl)benzamide is a synthetic organic compound characterized by its white crystalline appearance and a molecular formula of C9H5F6NO. With a molecular weight of 259.14 g/mol, this chemical is stable under normal conditions but may decompose when exposed to high temperatures. It is soluble in organic solvents such as ethanol and dichloromethane, while exhibiting limited solubility in water. Known for its use in the production of pharmaceuticals and agrochemicals, 2,5-Bis(trifluoromethyl)benzamide serves as a versatile building block in organic synthesis and has demonstrated antimicrobial and antifungal properties.

53130-46-4

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53130-46-4 Usage

Uses

Used in Pharmaceutical Industry:
2,5-Bis(trifluoromethyl)benzamide is used as a building block in the synthesis of various pharmaceutical compounds due to its unique chemical structure and reactivity. Its properties contribute to the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, 2,5-Bis(trifluoromethyl)benzamide is utilized as a key intermediate in the production of pesticides and other agrochemicals. Its incorporation aids in enhancing the effectiveness of these products in controlling pests and diseases in agriculture.
Used as Antimicrobial Agent:
2,5-Bis(trifluoromethyl)benzamide is employed as an antimicrobial agent for its ability to inhibit the growth of certain microorganisms. This application is beneficial in various industries where controlling microbial contamination is crucial.
Used as Antifungal Agent:
2,5-BIS(TRIFLUOROMETHYL)BENZAMIDE also serves as an antifungal agent, leveraging its properties to prevent the growth of fungi. This use is particularly relevant in medical and agricultural settings where fungal infections or infestations can be detrimental.

Check Digit Verification of cas no

The CAS Registry Mumber 53130-46-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,1,3 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 53130-46:
(7*5)+(6*3)+(5*1)+(4*3)+(3*0)+(2*4)+(1*6)=84
84 % 10 = 4
So 53130-46-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H5F6NO/c10-8(11,12)4-1-2-6(9(13,14)15)5(3-4)7(16)17/h1-3H,(H2,16,17)

53130-46-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-BIS(TRIFLUOROMETHYL)BENZAMIDE

1.2 Other means of identification

Product number -
Other names -

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:53130-46-4 SDS

53130-46-4Downstream Products

53130-46-4Relevant academic research and scientific papers

Stable and reusable nanoscale Fe2O3-catalyzed aerobic oxidation process for the selective synthesis of nitriles and primary amides

Murugesan, Kathiravan,Senthamarai, Thirusangumurugan,Sohail, Manzar,Sharif, Muhammad,Kalevaru, Narayana V.,Jagadeesh, Rajenahally V.

supporting information, p. 266 - 273 (2018/01/12)

The sustainable introduction of nitrogen moieties in the form of nitrile or amide groups in functionalized molecules is of fundamental interest because nitrogen-containing motifs are found in a large number of life science molecules, natural products and materials. Hence, the synthesis and functionalization of nitriles and amides from easily available starting materials using cost-effective catalysts and green reagents is highly desired. In this regard, herein we report the nanoscale iron oxide-catalyzed environmentally benign synthesis of nitriles and primary amides from aldehydes and aqueous ammonia in the presence of 1 bar O2 or air. Under mild reaction conditions, this iron-catalyzed aerobic oxidation process proceeds to synthesise functionalized and structurally diverse aromatic, aliphatic and heterocyclic nitriles. Additionally, applying this iron-based protocol, primary amides have also been prepared in a water medium.

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