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4-(Cyclopenta-2,4-dien-1-ylidenemethyl)-N,N-dimethylaniline is an organic compound with the chemical formula C15H17N. It is a derivative of aniline, featuring a cyclopentadienyl group attached to the 4-position of the aniline molecule. 4-(cyclopenta-2,4-dien-1-ylidenemethyl)-N,N-dimethylaniline is characterized by its aromatic structure, with the cyclopentadienyl ring contributing to its stability and reactivity. It is used in various chemical syntheses, particularly in the production of dyes and pigments, due to its ability to form stable chromophores. The compound's molecular structure allows for a range of applications in the chemical industry, including as an intermediate in the synthesis of more complex organic molecules.

2428-22-0

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2428-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2428-22-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2428-22:
(6*2)+(5*4)+(4*2)+(3*8)+(2*2)+(1*2)=70
70 % 10 = 0
So 2428-22-0 is a valid CAS Registry Number.

2428-22-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(cyclopenta-2,4-dien-1-ylidenemethyl)-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names 4-(2,4-Cyclopentadien-1-ylidenemethyl)-N,N-dimethylaniline

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:2428-22-0 SDS

2428-22-0Relevant academic research and scientific papers

Cyclopentadienyl-Based Anticancer Drugs: Improvement of Cytotoxic Activity through Functionalisation of the π Ligand

Absolonová, Monika,Melounková, Lucie,Vinklárek, Jaromír,Honzí?ek, Jan,Dostál, Libor,Mrózek, Ond?ej

, p. 1804 - 1812 (2021)

Cytotoxic complexes containing molybdenum are widely studied as a potential substitution for commercially used drugs that often suffer from pronounced side effects and cellular resistance. Compounds of the type [(η5-Cp′)Mo(CO)2(

Ring-functionalized niobocene complexes

Honzickova, Iva,Honzicek, Jan,Vinklarek, Jaromir,Padelkova, Zdenka,Rezacova, Martina,Sebestova, Lucie

, p. 252 - 258 (2014/04/03)

A series of new ring-functionalized niobocene dichloride compounds (RCH2C5H4)2NbCl2 (R = MeOCH2, (CH2)5NCH2, 2-MeOC 6H4, 3-MeOC6

Synthesis, characterization and cytotoxic activity on breast cancer cells of new half-titanocene derivatives

Sirignano, Esther,Saturnino, Carmela,Botta, Antonio,Sinicropi, Maria Stefania,Caruso, Anna,Pisano, Assunta,Lappano, Rosamaria,Maggiolini, Marcello,Longo, Pasquale

, p. 3458 - 3462 (2013/06/27)

A series of novel titanocene-complexes has been prepared and evaluated for their growth regulatory effects in MCF7 and SkBr3 breast cancer cells. The capability of some of these compound to elicit relevant repressive effects on cancer cell growth could be taken into account towards novel pharmacological approaches in cancer therapy.

An efficient catalytic method for fulvene synthesis

Cokun, Necdet,Erden, Ihsan

experimental part, p. 8607 - 8614 (2011/11/30)

The effects of the nature and amount of base, substrate structure, amount of added water and solvent on the condensation of carbonyl compounds with cyclopentadiene in the presence of secondary amines were investigated. Based on these studies, a new efficient and green synthesis of fulvenes was developed.

Novel titanocene anti-cancer drugs derived from fulvenes and titanium dichloride

Tacke, Matthias,Allen, Lorcan T.,Cuffe, Laurence,Gallagher, William M.,Lou, Ying,Mendoza, Oscar,Müller-Bunz, Helge,Rehmann, Franz-Josef K.,Sweeney, Nigel

, p. 2242 - 2249 (2007/10/03)

Starting from 6-(p-N,N-dimethylanilinyl)fulvene (1a) or 6-(pentamethylphenyl)fulvene (1b) [1,2-di(cyclopentadienyl)-1,2-di (p-N,N-dimethylaminophenyl)ethanediyl] titanium dichloride (2a) and [1,2-di(cyclopentadienyl)-1,2-bis(pentamethylphenyl)ethanediyl] titanium dichloride (2b) and their corresponding dithiocyanato complexes (3a, 3b) were synthesized. Titanocene 2b did not show a cytotoxic effect, but when 2a was tested against pig kidney carcinoma cells (LLC-PK) or human ovarian carcinoma cells (A2780/cp70) inhibitory concentrations (IC50) of 2.7 × 10-4 and 1.9 × 10-4 M, respectively, were observed.

Facile synthesis of 1,2-diaryl- and triarylethenes with supported fluoride bases

Hellwinkel,Goke,Karle

, p. 973 - 978 (2007/10/02)

Differently substituted arenecarbaldehydes, mainly benzaldehydes, can be very efficiently condensed with a wide variety of methylbenzenes having an electron-withdrawing group in the para-position, as well as with fluorenes, xanthene, cyclopentadienes and indenes by using a standardized KF- or CsF-Al2O3 base system in dimethylformamide.

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