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25753-22-4

2,4,6-Tris(trifluoromethyl)aniline is an organic compound characterized by the presence of three trifluoromethyl groups attached to the aniline molecule. 2,4,6-TRIS(TRIFLUOROMETHYL)ANILINE is known for its unique properties, such as increased stability and reactivity, which make it a valuable tool in various applications.

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  • 25753-22-4 Structure

  • Basic information

    1. Product Name: 2,4,6-TRIS(TRIFLUOROMETHYL)ANILINE
    2. Synonyms: 2,4,6-TRIS(TRIFLUOROMETHYL)ANILINE
    3. CAS NO:25753-22-4
    4. Molecular Formula: C9H4F9N
    5. Molecular Weight: 297.12
    6. EINECS: N/A
    7. Product Categories: Amines;Phenyls & Phenyl-Het;Phenyls & Phenyl-Het
    8. Mol File: 25753-22-4.mol

  • Chemical Properties

    1. Melting Point: 57-59
    2. Boiling Point: 149.8°C at 760 mmHg
    3. Flash Point: 55.5°C
    4. Appearance: /
    5. Density: 1.545g/cm3
    6. Vapor Pressure: 3.97mmHg at 25°C
    7. Refractive Index: 1.388
    8. Storage Temp.: Refrigerator, under inert atmosphere
    9. Solubility: Chloroform (Slightly), Methanol (Slightly)
    10. CAS DataBase Reference: 2,4,6-TRIS(TRIFLUOROMETHYL)ANILINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,4,6-TRIS(TRIFLUOROMETHYL)ANILINE(25753-22-4)
    12. EPA Substance Registry System: 2,4,6-TRIS(TRIFLUOROMETHYL)ANILINE(25753-22-4)

  • Safety Data

    1. Hazard Codes: Xi
    2. Statements: 36/37/38
    3. Safety Statements: 26-36/37/39
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 25753-22-4(Hazardous Substances Data)

25753-22-4 Usage

Uses

Used in Medical Chemistry:
2,4,6-Tris(trifluoromethyl)aniline is used as a valuable tool in medical chemistry due to its fluorinated substituents. These fluorinated groups enhance the compound's stability and reactivity, making it suitable for various pharmaceutical applications.
Used in the Preparation of Azo Dyes:
2,4,6-Tris(trifluoromethyl)aniline is also used in the preparation of azo dyes containing fluorine. The presence of fluorine in these dyes provides improved properties, such as increased color strength and resistance to fading, making them suitable for various industrial applications, including textiles, plastics, and printing inks.

Check Digit Verification of cas no

The CAS Registry Mumber 25753-22-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,5 and 3 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 25753-22:
(7*2)+(6*5)+(5*7)+(4*5)+(3*3)+(2*2)+(1*2)=114
114 % 10 = 4
So 25753-22-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H4F9N/c10-7(11,12)3-1-4(8(13,14)15)6(19)5(2-3)9(16,17)18/h1-2H,19H2

25753-22-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-TRIS(TRIFLUOROMETHYL)ANILINE

1.2 Other means of identification

Product number -
Other names 2',4',6'-Tris-(trifluormethyl)-anilin

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:25753-22-4 SDS

25753-22-4Relevant articles and documents

An expedient synthesis of 2,4,6-tris(trifluoromethyl)aniline

Edelbach, Brian L.,Pharoah, Blaze M.,Bellows, Sarina M.,Thayer, Peter R.,Fennie, Charles N.,Cowley, Ryan E.,Holland, Patrick L.

, p. 3595 - 3597 (2013/02/22)

A simple two-step synthetic route leads to 2,4,6-tris(trifluoromethyl) aniline. It proceeds through deprotonation and iodination of 1,3,5-tris(trifluoromethyl)benzene, followed by copper-catalyzed amination. Georg Thieme Verlag KG Stuttgart - New York.

Trifluoromethylation of various aromatic compounds by CF3I in the presence of Fe(II) compound, H2O2 and dimethylsulfoxide

Kino, Tatsuhito,Nagase, Yu,Ohtsuka, Yuhki,Yamamoto, Kyoko,Uraguchi, Daisuke,Tokuhisa, Kenji,Yamakawa, Tetsu

experimental part, p. 98 - 105 (2010/03/03)

Trifluoromethylation of aromatic and hetero-aromatic compounds by CF3I in the presence of Fe(II) compound, H2O2 and dimethylsulfoxide was investigated. Various trifluoromethylated benzene derivatives, six-membered nitrogen-containing aromatic compounds and five-membered hetero-aromatic compounds were obtained under mild conditions. General orientation of electrophilic substitution of aromatic compounds was observed similarly as reported in other radical trifluoromethylation previously.

Preparation and reactions of 2,4,6-tris(trifluoromethyl)phenylamine

Ahlemann, Jens-T,Roesky, Herbert W.,Noltemeyer, Mathias,Schmidt, Hans-G.,Markovsky, Leonid N.,Shermolovich, Yuri G.

, p. 87 - 90 (2007/10/03)

Starting from RfH (1) [Rf = 1,3,5-tris(trifluoromethyl)phenyl] RfNH2 (6) is obtained in a four-step synthesis. The amine 6 reacts with chlorotrimethylsilane in the presence of DBU (1,8-diazabicyclo(5,4,0)undec-7

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