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119001-43-3

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119001-43-3 Usage

Description

Tris(4-formylphenyl)amine is an organic compound characterized by its pale yellow powder form. It is a tris-aryl amine derivative featuring three 4-formylphenyl groups attached to an amine core. This unique structure endows it with specific chemical properties that make it suitable for various applications, particularly in the field of chemistry and materials science.

Uses

Used in Chemical Synthesis:
Tris(4-formylphenyl)amine is used as a key building block for the synthesis of complex organic molecules and materials. Its reactive formyl groups facilitate the formation of various chemical bonds, making it a versatile component in the creation of advanced chemical structures.
Used in the Preparation of Triangular Ligands:
Tris(4-formylphenyl)amine is utilized as a precursor in the preparation of triangular ligands, which are essential for the self-assembly of M4L4 tetrahedra. These tetrahedra are of significant interest in the field of supramolecular chemistry due to their unique structural properties and potential applications in catalysis, sensing, and drug delivery.
Used in Materials Science:
In the field of materials science, Tris(4-formylphenyl)amine is employed as a component in the development of novel materials with tailored properties. Its ability to form stable structures through its formyl groups allows for the creation of materials with enhanced stability, strength, and functionality.
Used in Pharmaceutical Industry:
Tris(4-formylphenyl)amine may also find applications in the pharmaceutical industry, where its unique chemical structure could be exploited for the design and synthesis of new drugs or drug delivery systems. Its potential use in this industry is still under exploration, and further research is needed to fully understand its capabilities and limitations.

Check Digit Verification of cas no

The CAS Registry Mumber 119001-43-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,0,0 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 119001-43:
(8*1)+(7*1)+(6*9)+(5*0)+(4*0)+(3*1)+(2*4)+(1*3)=83
83 % 10 = 3
So 119001-43-3 is a valid CAS Registry Number.
InChI:InChI=1/C21H15NO3/c23-13-16-1-7-19(8-2-16)22(20-9-3-17(14-24)4-10-20)21-11-5-18(15-25)6-12-21/h1-15H

119001-43-3 Well-known Company Product Price

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  • TCI America

  • (T2310)  Tris(4-formylphenyl)amine  >96.0%(HPLC)

  • 119001-43-3

  • 500mg

  • 935.00CNY

  • Detail
  • TCI America

  • (T2310)  Tris(4-formylphenyl)amine  >96.0%(HPLC)

  • 119001-43-3

  • 500mg

  • 935.00CNY

  • Detail
  • Aldrich

  • (679658)  Tris(4-formylphenyl)amine  97%

  • 119001-43-3

  • 679658-500MG

  • 1,115.01CNY

  • Detail
  • Aldrich

  • (679658)  Tris(4-formylphenyl)amine  97%

  • 119001-43-3

  • 679658-5G

  • 5,317.65CNY

  • Detail
  • TCI America

  • (T2310)  Tris(4-formylphenyl)amine  >96.0%(HPLC)

  • 119001-43-3

  • 500mg

  • 935.00CNY

  • Detail
  • TCI America

  • (T2310)  Tris(4-formylphenyl)amine  >96.0%(HPLC)

  • 119001-43-3

  • 500mg

  • 935.00CNY

  • Detail

119001-43-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name Tris(4-formylphenyl)amine

1.2 Other means of identification

Product number -
Other names 4,4',4''-Nitrilotribenzaldehyde

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:119001-43-3 SDS

119001-43-3Relevant articles and documents

Synthesis and optical properties of (A)n-π-(Ph)3N type dyes

Li, Xiaochuan,Kim, Sung-Hoon,Kun, Jun,Son, Young-A

, p. 164 - 172 (2009)

Two new (A)n-π-(Ph)3N type dyes were designed, synthesized and characterized. The optical properties and structures of them were studied, including UV-visible spectroscopy, photo-luminescence spectroscopy. The geometric structures of

A novel fluorescent sensor based on triphenylamine with AIE properties for the highly sensitive detection of CN?

Deng, Qinyue,Feng, Xicheng,Huang, Mingxian,Li, Denghui,Li, Wanfang,Liu, Lian,Zuo, Bin

, (2021)

In this study, a novel fluorescent sensor 1 built on triphenylamine was designed for the extremely sensitive detection of trace cyanide anions. The UV absorbance and fluorescence emission intensity of sensor 1 with aggregation-induced emission (AIE) prope

A direct crossed polymerization of triphenylamines and cyclohexanones: Via CC bond formation: The method and its bioimaging application

Ma, Hengchang,Cao, Haiying,Lei, Lei,Yang, Zengming,Yang, Manyi,Qin, Yanfang,Ma, Yucheng,Guan, Xiaolin,Lu, Dedai,Lei, Ziqiang

, p. 7908 - 7914 (2017)

The effective polymerization process is very desirable in the field of macromolecule science. In this study, we present a facile synthetic method via aldol addition and condensation (AAC) that leads to the formation of fluorescent linear and branched poly

Highly efficient deep-blue light-emitting material based on V-Shaped donor-acceptor triphenylamine-phenanthro[9,10-d]imidazole molecule

Gao, Yu,Li, Weijun,Liu, Haichao,Yang, Bing,Yu, Yue,Zhang, Shitong,Zhao, Ruiyang,Zhou, Changjiang

, (2020)

Based on novel phenanthro[9,10-d]imidazole (PI) chromophore, three deep-blue luminescent donor-acceptor molecules with different molecular configurations at the triphenylamine (TPA) core were designed and synthesized, the linear TPA-1PI, the V-shaped TPA-

In Situ Spectroelectrochemical Investigations of RuII Complexes with Bispyrazolyl Methane Triarylamine Ligands

Hua, Carol,Abrahams, Brendan F.,Tuna, Floriana,Collison, David,D'Alessandro, Deanna M.

, p. 546 - 555 (2017)

The synthesis and characterization of two triarylamine ligands, 4-(di(1H-pyrazol-1-yl)methyl)-N-(4-(di(1H-pyrazol-1-yl)methyl)phenyl)-N-phenylaniline (TPA-2bpm) and tris(4-(di(1H-pyrazol-1-yl)methyl)phenyl)amine (TPA-3bpm), containing the bispyrazolylmeth

Synthesis of hole-transporting hydrazone dendrimers

Nam, Haehyun,Kang, Dae Ho,Kim, Jai Kyeong,Park, Soo Young

, p. 1298 - 1299 (2000)

Hole-transporting aromatic hydrazone dendrimers were synthesized by convergent method. Structures of dendrimers were characterized by NMR, IR, GC/MS (FAB+), and elemental analysis.

Photoinitiators for two-photon polymerisation: effect of branching and viscosity on polymerisation thresholds

Whitby, Reece,Ben-Tal, Yael,MacMillan, Ryan,Janssens, Stefaan,Raymond, Sebastiampillai,Clarke, Dave,Jin, Jianyong,Kay, Andrew,Simpson, M. Cather

, p. 13232 - 13239 (2017)

A series of multi-branched two-photon photoinitiators (PIs) based around the well-known triphenylamine donor core were synthesised for use in two-photon polymerisation (TPP) and are designated as compounds 6, 7 and 8. The use of a phenylene-vinylene π-sys

Water-Soluble Fluorescent Probes for Selective Recognition of Lysine and Its Application in an Object Carry-and-Release System

Ma, Hengchang,Qi, Chunxuan,Cao, Haiying,Zhang, Zhongwei,Yang, Zengming,Zhang, Bing,Chen, Chao,Lei, Zi Qiang

, p. 58 - 63 (2016)

A water-soluble fluorescent probe PEG-TPA-5′ was synthesized, which shows an excellent selectivity to detect Lys in aqueous phase. An object carry-and-release system is established by applying PEG-TPA-5′ as carrier and Lys as chemical stimulating source.

Antibacterial activities of mono-, di- and tri-substituted triphenylamine-based phosphonium ionic liquids

Brunel, Frédéric,Lautard, Christelle,di Giorgio, Carole,Garzino, Frédéric,Raimundo, Jean-Manuel,Bolla, Jean-Michel,Camplo, Michel

, p. 926 - 929 (2018)

We report the synthesis of new mono, di and tri phosphonium ionic liquids and the evaluation of their antibacterial activities on both Gram-positive and Gram-negative bacteria from the ESKAPE-group. Among the molecules synthesized some of them reveal a st

Reinvestigation of the Vilsmeier-Haack Formylation of Triphenylamine

Lai, Gaifa,Bu, Xiu R.,Santos, Javier,Mintz, Eric A.

, p. 1275 - 1276 (1997)

Two previously claimed results on the Vilsmeier-Haack formylation of triphenylamine were demonstrated to be in error and the unambiguous reproducible procedures were developed to prepare 4-formyltriphenylamine (3) and 4,4'-diformyltriphenylamine (4), respectively, in good yields.

Efficient and straightforward click synthesis of structurally related dendritic triazoles

Mangione,Spanevello,Anzardi

, p. 47681 - 47688 (2017)

A simple, rapid and efficient copper-catalyzed 1,3-dipolar cycloaddition reaction is described for the synthesis of a novel family of twelve triazolic dendrimers structurally related. The products were the result of the click reaction of three cores and four different azides in tetrahydrofuran applying a homogeneous copper catalysis. The reaction intermediates and products were obtained in very good to excellent yields using straightforward and simple work-up procedures. This new family of compounds contain electroactive moieties such as carbazole and triphenylamine which may turn them into excellent candidates for the development of optoelectronic organic materials.

Sulfur rich electron donors-formation of singlet versus triplet radical ion pair states featuring different lifetimes in the same conjugate

Saha, Avishek,Chen, Muqing,Lederer, Marcus,Kahnt, Axel,Lu, Xing,Guldi, Dirk M.

, p. 1360 - 1368 (2017)

An unprecedented family of novel electron-donor acceptor conjugates based on fullerenes as electron acceptors, on one hand, and triphenyl amines as electron donors, on the other hand, have been synthesized and characterized in a variety of solvents using

Quantifying the nitrogen effect on CO2 capture using isoporous network polymers

Nguyen, Thien S.,Yavuz, Cafer T.

, p. 4273 - 4275 (2020)

The impact of nitrogen atoms on CO2 binding was evaluated for two isostructural porous bisimidazole-linked polymers (BILPs), which serendipitously had identical surface areas and pore size distributions, a very rare observation. The two structu

Multi-color electrochromism from coordination nanosheets based on a terpyridine-Fe(ii) complex

Kuai, Yu,Li, Weijun,Dong, Yujie,Wong, Wai-Yeung,Yan, Shuanma,Dai, Yuyu,Zhang, Cheng

, p. 15121 - 15126 (2019)

A metal complex nanosheet was synthesized by the liquid-liquid interface self-assembly method from a star-shaped ligand of tris[4-(4′-2,2′:6′,2′′-terpyridyl)-phenyl]amine in organic solvents and metal ion Fe(ii) in water solution. The as-prepared nanoshee

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