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87963-80-2

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87963-80-2 Usage

Description

4-DIMETHYLAMINOPHENYLAZOPHENYL-4'-MALEIM is a chemical compound that features a maleimide group attached to an azobenzene molecule, known for its bright red color and versatile applications in coloration and light-sensitive materials.

Uses

Used in Paints and Inks Industry:
4-DIMETHYLAMINOPHENYLAZOPHENYL-4'-MALEIM is used as a dye and pigment for its bright red color, contributing to the production of red pigments in paints and inks.
Used in Plastics Industry:
In the plastics industry, 4-DIMETHYLAMINOPHENYLAZOPHENYL-4'-MALEIM serves as a colorant, providing a vibrant red hue to various plastic products.
Used in Photodynamic Therapy:
4-DIMETHYLAMINOPHENYLAZOPHENYL-4'-MALEIM is studied for its potential use as a photosensitive compound in photodynamic therapy, a cancer treatment that utilizes light and a photosensitive agent to destroy cancer cells.
Used in Light-Sensitive Materials:
Due to its ability to undergo photoisomerization and photocleavage reactions, 4-DIMETHYLAMINOPHENYLAZOPHENYL-4'-MALEIM is used in the development of light-sensitive materials, which can change properties or structure upon exposure to light.

Check Digit Verification of cas no

The CAS Registry Mumber 87963-80-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,9,6 and 3 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 87963-80:
(7*8)+(6*7)+(5*9)+(4*6)+(3*3)+(2*8)+(1*0)=192
192 % 10 = 2
So 87963-80-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H16N4O2/c1-21(2)15-7-3-13(4-8-15)19-20-14-5-9-16(10-6-14)22-17(23)11-12-18(22)24/h3-12H,1-2H3/b20-19+

87963-80-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[4-[[4-(dimethylamino)phenyl]diazenyl]phenyl]pyrrole-2,5-dione

1.2 Other means of identification

Product number -
Other names 4-Dimethylaminophenylazophenyl-4'-maleimide

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:87963-80-2 SDS

87963-80-2Downstream Products

87963-80-2Relevant articles and documents

Molecular length adjustment for organic azo-based nonvolatile ternary memory devices

Miao, Shifeng,Li, Hua,Xu, Qingfeng,Li, Najun,Zheng, Junwei,Sun, Ru,Lu, Jianmei,Li, Chang Ming

, p. 16582 - 16589 (2012/09/05)

Two conjugated small molecules with different molecular length, DPAPIT and DPAPPD, in which an electron donor dimethylamino moiety and an electron acceptor phthalimide core unit are bridged by another electron-accepting azobenzene block, were designed and synthesized. DPAPIT molecule with longer conjugation length stacked regularly in the solid state and formed uniform nanocrystalline film. The fabricated memory devices with DPAPIT as active material exhibited outstanding nonvolatile ternary memory effect with the current ratio of ~1:101.7:104 for "0", "1" and "2" states and all the switching threshold voltages lower than -3 V. In contrast, the shorter molecule DPAPPD showed amorphous microstructure and no obvious conductive switching behavior was observed in the device. The crystallinity and surface roughness of DPAPIT thin films were significantly improved as the annealing temperature increased, lowering the switching threshold voltages which are highly desirable for low-power consumption data-storage devices. It is worth noting that the tristable memory signals of DPAPIT film could also be achieved by using conductive atomic force microscopy with platinum-coated probe, which enables fabrication of nano-scale or even molecular-scale device, a significant progress for the ultra-high density data storage application. Mechanism analysis demonstrated that two charge traps with different depth in the molecular backbone were injected by charge carriers progressively as the external bias increased, resulting in the formation of three distinct conductive states (OFF, ON1 and ON2 states). The Royal Society of Chemistry 2012.

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