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Benzenamine, N-(1,2-diphenylethylidene)-, also known as N-(1,2-diphenylethylidene)aniline or Michler's ketone, is an organic compound with the chemical formula C20H17N. It is a yellow crystalline solid that is soluble in organic solvents and slightly soluble in water. Benzenamine, N-(1,2-diphenylethylidene)- is derived from benzenamine (aniline) and features a 1,2-diphenylethylidene group attached to the nitrogen atom. Michler's ketone is primarily used as a dyestuff intermediate, particularly in the production of azo dyes, and has applications in the synthesis of various pigments and pharmaceuticals. It is also employed as a fluorescence brightening agent and a reagent in chemical analysis. Due to its potential health and environmental risks, handling and disposal of Michler's ketone must be done with proper safety measures.

3723-13-5

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3723-13-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3723-13-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,2 and 3 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 3723-13:
(6*3)+(5*7)+(4*2)+(3*3)+(2*1)+(1*3)=75
75 % 10 = 5
So 3723-13-5 is a valid CAS Registry Number.

3723-13-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(1,2-Diphenylethylidene)aniline

1.2 Other means of identification

Product number -
Other names Bibenzyl-α-yliden-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:3723-13-5 SDS

3723-13-5Relevant academic research and scientific papers

Reversible Vapochromic Luminescence Accompanied by Planar Half-Chair Conformational Change of a Propeller-Shaped Boron β-Diketiminate Complex

Ito, Shunichiro,Yaegashi, Misao,Tanaka, Kazuo,Chujo, Yoshiki

, p. 9302 - 9312 (2021)

Leakage of volatile organic compounds (VOCs) is one of the most severe industrial problems, because it can cause environmental pollution, global warming, fire, and explosion. Hence, the visualization of leakage is an essential technology to detect it at a

Towards the rational design of ylide-substituted phosphines for gold(i)-catalysis: From inactive to ppm-level catalysis

Handelmann, Jens,Babu, Chatla Naga,Steinert, Henning,Schwarz, Christopher,Scherpf, Thorsten,Kroll, Alexander,Gessner, Viktoria H.

, p. 4329 - 4337 (2021/04/12)

The implementation of gold catalysis into large-scale processes suffers from the fact that most reactions still require high catalyst loadings to achieve efficient catalysis thus making upscaling impractical. Here, we report systematic studies on the impa

Iron-catalysed 1,2-aryl migration of tertiary azides

Wei, Kaijie,Yang, Tonghao,Chen, Qing,Liang, Siyu,Yu, Wei

supporting information, p. 11685 - 11688 (2020/10/19)

1,2-Aryl migration of α,α-diaryl tertiary azides was achieved by using the catalytic system of FeCl2/N-heterocyclic carbene (NHC) SIPr·HCl. The reaction generated aniline products in good yields after one-pot reduction of the migration-resultant imines.

Mono- and diylide-substituted phosphines (YPhos): Impact of the ligand properties on the catalytic activity in gold(i)-catalysed hydroaminations

Schwarz, Christopher,Handelmann, Jens,Baier, Daniel M.,Ouissa, Alina,Gessner, Viktoria H.

, p. 6808 - 6815 (2019/12/03)

Understanding the impact of ligand properties on their performance in catalysis is seminal for future ligand design and catalyst improvement. In this work, the influence of the steric and electronic properties on the efficiency of a series of mono- and di

A silica-supported titanium catalyst for heterogeneous hydroamination and multicomponent coupling reactions

Aldrich, Kelly E.,Odom, Aaron L.

, p. 11352 - 11360 (2019/08/07)

Highly dehydrated silica gel, SiO2700, gave a material with a total surface hydroxyl density of 0.31 ± 0.05 mmol g-1, 0.9 ± 0.1 Si-OH sites per nm2. Treatment of this material with Ti(NMe2)4/sub

Ylide-Functionalized Phosphines: Strong Donor Ligands for Homogeneous Catalysis

Scherpf, Thorsten,Schwarz, Christopher,Scharf, Lennart T.,Zur, Jana-Alina,Helbig, Andreas,Gessner, Viktoria H.

supporting information, p. 12859 - 12864 (2018/09/25)

Phosphines are important ligands in homogenous catalysis and have been crucial for many advances, such as in cross-coupling, hydrofunctionalization, or hydrogenation reactions. Herein we report the synthesis and application of a novel class of phosphines bearing ylide substituents. These phosphines are easily accessible via different synthetic routes from commercially available starting materials. Owing to the extra donation from the ylide group to the phosphorus center the ligands are unusually electron-rich and can thus function as strong electron donors. The donor capacity surpasses that of commonly used phosphines and carbenes and can easily be tuned by changing the substitution pattern at the ylidic carbon atom. The huge potential of ylide-functionalized phosphines in catalysis is demonstrated by their use in gold catalysis. Excellent performance at low catalyst loadings under mild reaction conditions is thus seen in different types of transformations.

Titanium-Catalyzed Hydroamination and Multicomponent Coupling with a Simple Silica-Supported Catalyst

Aldrich, Kelly E.,Odom, Aaron L.

, p. 4341 - 4349 (2019/01/03)

Hydroamination and multicomponent coupling reactions catalyzed by homogeneous Ti(IV) complexes can produce valuable imines, amines, and other nitrogen-containing organic building blocks. Typically catalysts for this transformation are very sensitive to an

Copper-Catalyzed Cascade Cycloamination of α-Csp3-H Bond of N-Aryl Ketimines with Azides: Access to Quinoxalines

Chen, Tengfei,Chen, Xun,Wei, Jun,Lin, Dongen,Xie, Ying,Zeng, Wei

supporting information, p. 2078 - 2081 (2016/06/01)

A copper-catalyzed cycloamination of α-Csp3-H bond of N-aryl ketimines with sodium azide has been developed. This methodology provides an efficient access to quinoxalines and features mild reaction conditions and readily available ketimines with diverse functional group tolerance.

Zirconium complexes stabilized by amine-bridged bis(phenolato) ligands as precatalysts for intermolecular hydroamination reactions

Sun, Qiu,Wang, Yaorong,Yuan, Dan,Yao, Yingming,Shen, Qi

, p. 20352 - 20360 (2015/12/04)

A series of zirconium complexes bearing amine-bridged bis(phenolato) ligands of different steric and electronic properties have been synthesized, and their activities in catalyzing intermolecular hydroamination reactions have been studied and compared. In

Synthesis of 1,2-borazaronaphthalenes from imines by base-promoted borylation of C-H bond

Liu, Xinwang,Wu, Pengbo,Li, Jianfeng,Cui, Chunming

, p. 3737 - 3744 (2015/05/05)

A new route from benzylic imines permits the synthesis of 1,2-borazaronaphthalenes in good yields. The reaction involves formation of the enamidyl dibromoborane, which undergoes base-promoted borylation of the nearby aromatic C-H bond. Electrophilic attack of the boron species onto the benzylic arene is supported by the slow borylation of arenes substituted with electron-withdrawing groups. The resultant boron bromides can be easily substituted with lithium reagents to provide a range of products. The electronic properties of these 1,2-borazaronaphthalene derivatives have been investigated by UV-vis and fluorescence spectroscopy.

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