4316-53-4

Basic information

• Product Name: 4-Methyltriphenylamine
• Synonyms: 4—METHYLTRIPHENYLAMINE;4-Tolyldiphenylamine;4-METHYLTRIPHENYLAMINE,98.0+%(GC);N,N-Diphenyl-p-toluidine;N-(4-Methylphenyl)diphenylamine;Diphenyl p-tolylamine;Diphenyl(4-methylphenyl)amine;Diphenyl(p-methylphenyl)amine
• CAS NO: 4316-53-4
• Molecular Formula: C₁₉H₁₇N
• Molecular Weight: 259.34
• EINECS: 1533716-785-6
• Product Categories: electronic;Acid Anhydrides, etc. (Reagents for Conducting Polymer Research);Functional Materials;Reagents for Conducting Polymer Research
• Mol File: 4316-53-4.mol
• Article Data: 85

Chemical Properties

• Melting Point: 67 °C
• Boiling Point: 393.8 °C at 760 mmHg
• Flash Point: 171.8 °C
• Appearance: /
• Density: 1.095 g/cm³
• Vapor Pressure: 2.08E-06mmHg at 25°C
• Refractive Index: 1.636
• Solubility: soluble in Toluene
• PKA: -2.62±0.30(Predicted)
• CAS DataBase Reference: 4-Methyltriphenylamine(CAS DataBase Reference)
• NIST Chemistry Reference: 4-Methyltriphenylamine(4316-53-4)
• EPA Substance Registry System: 4-Methyltriphenylamine(4316-53-4)

Safety Data

• Hazardous Substances Data: 4316-53-4(Hazardous Substances Data)

Usage

Description

4-Methyltriphenylamine, with the CAS number 4316-53-4, is an organic compound that belongs to the triphenylamine family. It is characterized by its molecular structure, which consists of a central nitrogen atom bonded to three phenyl rings, with one of the phenyl rings having a methyl group attached to it. 4-Methyltriphenylamine is known for its reactivity and versatility in various organic reactions and synthesis processes.

Uses

Used in Organic Synthesis:
4-Methyltriphenylamine is used as a reactant and reagent in organic synthesis for its ability to participate in a wide range of chemical reactions. Its unique structure allows it to act as a building block for the creation of more complex organic molecules, which can be utilized in various applications across different industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4-Methyltriphenylamine is used as a reactant for the synthesis of various drug molecules. Its reactivity and structural properties make it a valuable component in the development of new medications, potentially contributing to the treatment of various diseases and health conditions.
Used in Chemical Research:
4-Methyltriphenylamine is also used in chemical research as a reagent for studying the properties and behavior of organic compounds. Its involvement in various chemical reactions provides valuable insights into the mechanisms and pathways of organic synthesis, which can be applied to the development of new materials and technologies.
Used in Material Science:
In the field of material science, 4-Methyltriphenylamine can be used as a component in the development of advanced materials with specific properties. Its incorporation into the molecular structure of these materials can lead to enhanced performance characteristics, such as improved conductivity, stability, or reactivity, depending on the desired application.

InChI:InChI=1/C19H17N/c1-16-12-14-19(15-13-16)20(17-8-4-2-5-9-17)18-10-6-3-7-11-18/h2-15H,1H3

Upstream product

• 624-31-7 4-tolyl iodide 
• 122-39-4 diphenylamine 
• 591-50-4 iodobenzene 
• 591-17-3 meta-bromotoluene 
• 106-38-7 para-bromotoluene 
• 99-99-0 1-methyl-4-nitrobenzene 
• 106-43-4 para-chlorotoluene 
• 106-49-0 p-toluidine 
• 108-86-1 bromobenzene 
• 62-53-3 aniline 
• 1821-36-9 N-phenyl-2-cyclohexylamine 
• 1132-38-3 N-cyclohexylidenebenzenamine 
• 12775-96-1 copper 
• 95-50-1 1,2-dichloro-benzene 

Downstream Products

• 100308-67-6 4,4′-dibromo-4′′-methyltriphenylamine 
• 20441-06-9 N,N'-di(4''-methylphenyl)-N,N'-diphenyl-1,1'-biphenyl-4,4'-diamine 
• 404825-34-9 N,N-di(4-iodophenyl)-4-tolylamine 
• 183994-94-7 4-(N,N-diphenylamino)benzyl bromide 
• 122112-54-3 4-[(4-formylphenyl)(4-methylphenyl)amino]benzaldehyde 
• 89115-21-9 4-(N-(4-methylphenyl)-N-phenylamino)benzaldehyde 
• 1233934-04-7 4-methyl-N,N-bis(4-(9-(3,4,5-trifluorophenyl)-9H-fluoren-9-yl)phenyl)aniline 
• 1233933-99-7 4-methyl-N,N-bis(4-(9-(4-fluorophenyl)-9H-fluoren-9-yl)phenyl)aniline 
• 1235971-60-4 4-methyl-N,N-bis-(4-(9-p-tolyl-9H-fluoren-9-yl)phenyl)aniline 
• 1235971-59-1 4-methyl-N,N-bis-(4-(9-(naphthalen-1-yl)-9H-fluoren-9-yl)phenyl)aniline 
• 1233934-00-3 4-methyl-N,N-bis-(4-(9-(4-tert-butylphen-yl)-9H-fluoren-9-yl)phenyl)aniline 
• 1233934-02-5 4-methyl-N,N-bis(4-(9-(4-(trifluoromethyl)-phenyl)-9H-fluoren-9-yl)phenyl)aniline 
• 1233934-01-4 4-methyl-N,N-bis(4-(2,7-dibromo-9-p-tolyl-9H-fluoren-9-yl)phenyl)aniline 
• 100803-48-3 N,N-bis[4-(2,2-diphenylethenyl)phenyl]-4-methylaniline 

Relevant articles and documents

A copper(ii) complex as an intermediate of copper(i)-catalyzed C-N cross coupling of N-phenylaniline with aryl halide by in situ ESI-MS study

Complexes [Cu(NPh2)2]-, [Cu(NPh 2)I]- and K[Cu(phen)(NPh2) (p-tolyl)] + were observed by in situ electrospray ionization mass spectrometry (ESI-MS) analysis of the copper(i)-cata

Design of Benzimidazolyl Phosphines Bearing AlterableP,OorP,N-Coordination: Synthesis, Characterization, and Insights into Their Reactivity

A new series of hemilabile benzimidazolyl phosphines is reported. Entities in this ligand family can be easily assembled and prepared on a large scale via a simple one-pot procedure. X-ray crystallographic analyses show that the Pd metal center can coordinate in different fashions, where it relies on the size of the ?PR2group. With the same ligand scaffold, the ligand having a ?PCy2moiety displays better efficiency in expediting aromatic C-C bond-coupling reactions, while the ligand associated with a ?P-t-Bu2group, in contrast, promotes C-N bond-forming reactions.

DIARYL AMINE COMPOUND AND METHOD FOR PRODUCING THE SAME

The present invention relates to a process for the preparation of diaryl amine compounds. A compound represented by chemical formula 1, a compound represented by chemical formula 2, and a synthetic reagent in a solvent, the synthetic reagent being CsF, KF, 18 - crown -6, K. 2 CO3, [TBAT] The present invention relates to a process for the preparation of diaryl amine compounds comprising a material selected from the group consisting of a (tetrabutylammonium difluorotriphenylsilicate), TBAF (tetrabutylammonium fluoride) and combinations thereof. Chemical Formula 1. Chemical Formula 2. The diaryl amine compound can be synthesized under the absence of a transition metal to be used to synthesize diaryl amine compounds having various substituents.

PHOSPHINE COMPOUND, CROSSLINKED COMPOSITION, AND MANUFACTURING METHOD OF AROMATIC AMINE COMPOUND

PROBLEM TO BE SOLVED: To provide a phosphine compound capable of constituting a transition metal complex excellent in reaction speed and selectivity as a catalyst. SOLUTION: There is provided a phosphine compound represented by the formula (I). In the formula Ar represents each independently an aryl group which may be substituted, R1 represents each independently a linear, branched or cyclic alkyl group, R2 represents each independently a linear, branched or cyclic alkyl group, alkoxy group or aryl group which may be substituted, or neighboring 2 R2 are bound each other to form a ring, and n represents an integer of 0 to 4. SELECTED DRAWING: None COPYRIGHT: (C)2020,JPOandINPIT