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89482-98-4

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89482-98-4 Usage

Description

bis[4-(dimethylamino)phenyl]methylidenepropanedinitrile, with the molecular formula C19H20N4, is a chemical compound that exhibits strong light absorption and emission properties. It is commonly utilized as a fluorescent dye in various scientific and industrial applications due to its ability to enhance electrical conductivity and light emission.

Uses

Used in Biological and Medical Research:
bis[4-(dimethylamino)phenyl]methylidenepropanedinitrile is used as a fluorescent dye for labeling and imaging applications in biological and medical research. Its strong light absorption and emission properties make it an ideal candidate for these purposes, allowing for the efficient tracking and visualization of biological processes and structures.
Used in Organic Semiconductors Manufacturing:
In the field of organic semiconductors, bis[4-(dimethylamino)phenyl]methylidenepropanedinitrile is used as a key component to improve the electrical conductivity and light emission of these materials. Its incorporation into organic semiconductors enhances their performance, making them more suitable for a range of applications, including flexible electronics and energy-efficient devices.
Used in Light-Emitting Diodes (LEDs) Production:
bis[4-(dimethylamino)phenyl]methylidenepropanedinitrile is also used in the manufacturing of light-emitting diodes (LEDs). Its ability to enhance light emission and electrical conductivity makes it a valuable addition to the production of LEDs, leading to more efficient and longer-lasting lighting solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 89482-98-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,8 and 2 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89482-98:
(7*8)+(6*9)+(5*4)+(4*8)+(3*2)+(2*9)+(1*8)=194
194 % 10 = 4
So 89482-98-4 is a valid CAS Registry Number.

89482-98-4SDS

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 2-[bis[4-(dimethylamino)phenyl]methylidene]propanedinitrile

1.2 Other means of identification

Product number -
Other names 1,1-Dicyan-2,2-bis-(4-dimethylaminophenyl)-ethylen

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:89482-98-4 SDS

89482-98-4Downstream Products

89482-98-4Relevant articles and documents

Silver(I) Ion Mediatied Desulfurization-Condensation of Thiocarbonyl Compounds with Several Nucleophiles

Shibuya, Isao,Taguchi, Yoichi,Tsuchiya, Tohru,Oishi, Akihiro,Katoh, Eisaku

, p. 3048 - 3052 (2007/10/02)

The desulfurization-condensation reaction was investigated in the presence of silver(I) salt for several kinds of thiocarbonyl compounds with nucleophiles.Such thiocarbonyl compounds as 4,4'-bis(dimethylamino)thiobenzophenone, ethylene trithiocarbonate, and N-(thiobenzoyl)morpholine react with malononitrile or other active methylene compounds in the presence of silver trifluoroacetate to afford the corresponding olefinic compounds together with silver sulfide.This reaction of thiocarbonyl compounds with some other nucleophiles such as aniline derivatives and ethylene glycol, has also afforded imines and 1,3-dioxolane derivatives.

Mass Spectra of Dicyanomethylene Derivatives of Benzophenone Analogs

Wang, Ching-Bore,Her, Guor-Rong,Watson, J. Throck

, p. 457 - 461 (2007/10/02)

The dicyanomethylene derivative of a benzophenone analog significantly alters the fragmentation pattern observed during electron impact ionization of the underivatized parent compound.A double bond connecting the dicyanomethylene moiety to the parent comp

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