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Benzenamine, 4,4'-[(4-fluorophenyl)methylene]bis[N,N-dimethyl-] is a complex organic compound with the chemical formula C20H20FN2. It is a derivative of benzenamine, also known as aniline, which is a primary aromatic amine. The compound features a central methylene bridge connecting two benzene rings, each substituted with a fluorine atom at the para position. Additionally, each nitrogen atom in the benzenamine groups is alkylated with two methyl groups, making it a dimethyl derivative. Benzenamine, 4,4'-[(4-fluorophenyl)methylene]bis[N,N-dimethyl- is characterized by its molecular structure, which includes fluorine substitution and N,N-dimethylation, and is often used in the synthesis of various pharmaceuticals and chemical intermediates due to its unique reactivity and properties.

3110-14-3

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3110-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3110-14-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,1,1 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3110-14:
(6*3)+(5*1)+(4*1)+(3*0)+(2*1)+(1*4)=33
33 % 10 = 3
So 3110-14-3 is a valid CAS Registry Number.

3110-14-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[[4-(dimethylamino)phenyl]-(4-fluorophenyl)methyl]-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names 4.4'-Dimethylamino-4''fluorotriphenylmethan

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:3110-14-3 SDS

3110-14-3Relevant academic research and scientific papers

An efficient and convenient protocol for the synthesis of diaminotriarylmethanes

Hou, Jun-Tao,Gao, Jian-Wu,Zhang, Zhan-Hui

experimental part, p. 495 - 499 (2011/12/16)

A novel and efficient procedure was developed for the preparation of diaminotriarylmethanes through the Baeyer condensation of aromatic aldehydes and N,N-dimethylaniline or N,N-diethylaniline in the presence of niobium chloride under solvent-free conditio

SbCl3-catalyzed one-pot synthesis of 4,4′-diamino- triarylmethanes under solvent-free conditions: Synthesis, characterization, and DFT studies

Bardajee, Ghasem Rezanejade

experimental part, p. 135 - 144 (2011/05/16)

A simple, efficient, and mild procedure for a solvent-free one-step synthesis of various 4,4′-diaminotriarylmethane derivatives in the presence of antimony trichloride as catalyst is described. Triarylmethane derivatives were prepared in good to excellent yields and characterized by elemental analysis, FTIR, 1H and 13C NMR spectroscopic techniques. The structural and vibrational analysis were investigated by performing theoretical calculations at the HF and DFT levels of theory by standard 6-31Gs *, 6-31G*/B3LYP, and B3LYP/cc-pVDZ methods and good agreement was obtained between experimental and theoretical results.

ZrOCl2 catalyzed Baeyer condensation: A facile and efficient synthesis of triarylmethanes under solvent-free conditions

Reddy, Ch Sanjeeva,Nagaraj,Srinivas,Reddy

experimental part, p. 248 - 254 (2009/12/03)

A facile and efficient synthesis of an array of triarylmethanes by the Baeyer condensation of different arylaldehydes carrying activated and deactivated groups and N,N-dimethyIaniline using a catalytic amount of ZrOCI2 under solvent-free microwave irradiation conditions is described. Further, the catalytic activity of ZrOCI2 is compared with traditional Lewis acid catalysts and found that this synthetic method has the advantages of excellent yields (70-96%), shorter reaction time (few minutes) and solvent-free conditions.

Fluorinated analogs of malachite green: Synthesis and toxicity

Kraus, George A.,Jeon, Insik,Nilsen-Hamilton, Marit,Awad, Ahmed M.,Banerjee, Jayeeta,Parvin, Bahram

, p. 986 - 994 (2008/09/20)

A series of fluorinated analogs of malachite green (MG) have been synthesized and their toxicity to Saccharomyces cerevisiae and a human ovarian epithelial cell line examined. The toxicity profiles were found to be different for these two species. Two ana

Color intensity control in polymers using triarylmethane leuconitriles as color formers

Malpert, John H,Grinevich, Oleg,Strehmel, Bernd,Jarikov, Viktor,Mejiritski, Alexander,Neckers, Douglas C

, p. 967 - 974 (2007/10/03)

Several triarylmethane leuconitriles have been synthesized. Color formation rates of triarylmethane dyes from corresponding leuconitriles have been compared in various media. Routes to color-on-demand processes are discussed.

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