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87963-80-2

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87963-80-2 Usage

General Description

4-DIMETHYLAMINOPHENYLAZOPHENYL-4'-MALEIM is a chemical compound commonly used as a dye and pigment in various industries. It is composed of a maleimide group attached to a azobenzene molecule, making it a versatile compound with applications in coloration and light-sensitive materials. It is known for its bright red color and is often used in making red pigments for paints, inks, and plastics. Additionally, this compound has been studied for potential use in photodynamic therapy, a treatment for certain types of cancer that uses light and a photosensitive compound to kill cancer cells. Due to its azo and maleimide groups, it can undergo photoisomerization and photocleavage reactions, making it potentially useful in light-sensitive materials and applications. Overall, 4-DIMETHYLAMINOPHENYLAZOPHENYL-4'-MALEIM is a versatile and multifunctional compound with various industrial and medical applications.

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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