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2,2-Bis-(4-aminophenyl)adamantane, also known as bis(4-aminophenyl)adamantane or BAPOA, is an organic chemical compound characterized by its rigid, polycyclic structure. It features two adamantane rings linked together, with two 4-aminophenyl groups attached to the central carbon atom, resulting in a molecular formula of C30H30N2. This unique structure endows BAPOA with specific properties that make it valuable in various applications.

164396-23-0

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164396-23-0 Usage

Uses

Used in Epoxy Resin Industry:
2,2-Bis-(4-aminophenyl)adamantane is used as a curing agent for epoxy resins, where it functions as a hardener and crosslinking agent. This role enhances the overall strength and durability of the material, making it suitable for a wide range of applications.
Used in Fiber-Reinforced Composites:
In the production of fiber-reinforced composites, 2,2-Bis-(4-aminophenyl)adamantane is utilized to improve the mechanical properties and performance of the composite materials, contributing to their structural integrity and reliability.
Used in Coatings Industry:
As a component in coatings, 2,2-Bis-(4-aminophenyl)adamantane is employed to increase the hardness, adhesion, and chemical resistance of the coating, providing a robust protective layer for various surfaces.
Used in Adhesives Industry:
In the formulation of adhesives, 2,2-Bis-(4-aminophenyl)adamantane serves to enhance the bonding strength and durability of the adhesive, ensuring strong and long-lasting adhesion between different materials.
Used in Organic Electronics:
2,2-Bis-(4-aminophenyl)adamantane has potential applications in the field of organic electronics, where its unique structure and properties can be leveraged to improve the performance of electronic devices and components.
Used in Optoelectronic Devices:
Similarly, in optoelectronic devices, 2,2-Bis-(4-aminophenyl)adamantane can be utilized to enhance the efficiency and functionality of these devices, taking advantage of its specific characteristics to optimize their performance.

Check Digit Verification of cas no

The CAS Registry Mumber 164396-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,4,3,9 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 164396-23:
(8*1)+(7*6)+(6*4)+(5*3)+(4*9)+(3*6)+(2*2)+(1*3)=150
150 % 10 = 0
So 164396-23-0 is a valid CAS Registry Number.

164396-23-0Relevant academic research and scientific papers

Synthesis and properties of ultralow dielectric porous polyimide films containing adamantane

Lv, Pengxia,Dong, Zhixin,Dai, Xuemin,Wang, Hanfu,Qiu, Xuepeng

, p. 549 - 559 (2018)

A series of novel ultralow dielectric porous polyimide (PI) films containing adamantane groups was prepared via the thermolysis of polyethylene glycol (PEG) oligomers mixed into PI matrix. Scanning electron microscopy results indicated that the porous PI

Simply structured, deep-blue phosphorescent organic light-emitting diode with bipolar host material

Fukagawa, Hirohiko,Irisa, Shiro,Hanashima, Hiromu,Shimizu, Takahisa,Tokito, Shizuo,Yokoyama, Norimasa,Fujikake, Hideo

, p. 1638 - 1643 (2011)

We developed an efficient, deep-blue phosphorescent organic light-emitting diode (POLED) with a simplified device structure using a new host material. There are only three organic layers in the deep-blue POLED, namely, a hole-transporting layer, an emitti

Compound, display panel and display device

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Paragraph 0098-0101, (2019/08/01)

The invention provides a compound with a D-(pi)-sigma-(pi)-A chemical structure. The compound has a chemical structure shown as formula (I), wherein L1 and L2 are selected from at least one of a single bond, C1-C20 alkylene, C3-C20 cycloalkylene, C3-C20 h

Guanidine-guanidinium cooperation in bifunctional artificial phosphodiesterases based on diphenylmethane spacers; Gem -dialkyl effect on catalytic efficiency

Salvio, Riccardo,Mandolini, Luigi,Savelli, Claudia

, p. 7259 - 7263 (2013/08/23)

Diphenylmethane derivatives 1-3, decorated with two guanidine units, are effective catalysts of HPNP transesterification. Substitution of the methylene group of the parent diphenylmethane spacer with cyclohexylidene and adamantylidene moieties enhances catalytic efficency, with gem-dialkyl effect accelerations of 4.5 and 9.1, respectively. Activation parameters and DFT calculations of the rotational barriers around the C-Ar bonds indicate that a major contribution to the driving force for enhanced catalysis is entropic in nature.

Pyridoindole derivative as electron transporting host material for efficient deep-blue phosphorescent organic light-emitting diodes

Fukagawa, Hirohiko,Yokoyama, Norimasa,Irisa, Shiro,Tokito, Shizuo

scheme or table, p. 4775 - 4778 (2012/02/01)

An electron-transporting host material suitable for deep-blue phosphorescent organic light-emitting diodes has been developed. The material exhibits electron-transport characteristics, high triplet energy, and high thermal stability. It is designed by int

Aromatic diamine compounds

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, (2008/06/13)

An aromatic diamine compound represented by formula (1): STR1 wherein R1 and R2, which may be the same or different, are each a hydrogen atom or a lower alkyl group; and an aromatic diamine compound useful as an intermediate for the

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