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6,12-Chrysenediamine, N,N,N',N'-tetraphenylis a chemical compound with the molecular formula C44H30N2. It is a diamine derivative of chrysene, a polycyclic aromatic hydrocarbon. 6,12-Chrysenediamine, N,N,N',N'-tetraphenylis known for its potential applications in the synthesis of various organic compounds, polymers, and organic electronic devices, as well as its pharmacological activities, including antimicrobial and anticancer properties. However, it requires careful handling due to potential risks to human health and the environment.

279672-22-9

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279672-22-9 Usage

Uses

Used in Organic Synthesis:
6,12-Chrysenediamine, N,N,N',N'-tetraphenylis used as a building block in the synthesis of various organic compounds and polymers. Its unique structure and reactivity make it a valuable component in the development of new materials with specific properties.
Used in Light-Emitting Polymers and Organic Electronic Devices:
6,12-Chrysenediamine, N,N,N',N'-tetraphenylhas been studied for its potential use in the production of light-emitting polymers and organic electronic devices. Its electronic properties and compatibility with other materials make it a promising candidate for these applications.
Used in Pharmaceutical Research:
6,12-Chrysenediamine, N,N,N',N'-tetraphenylhas been investigated for its potential pharmacological activities, particularly its antimicrobial and anticancer properties. Its unique chemical structure may offer new avenues for the development of therapeutic agents.
Used in Antimicrobial Applications:
6,12-Chrysenediamine, N,N,N',N'-tetraphenylis used as an antimicrobial agent, exhibiting activity against various types of bacteria and other microorganisms. Its ability to disrupt microbial processes makes it a potential candidate for use in antimicrobial formulations.
Used in Anticancer Applications:
6,12-Chrysenediamine, N,N,N',N'-tetraphenylis being studied for its potential as an anticancer agent. Its ability to interact with cellular processes and inhibit the growth of cancer cells makes it a promising candidate for further research and development in oncology.
Used in Environmental and Health Risk Assessment:
Due to its potential risks to human health and the environment, 6,12-Chrysenediamine, N,N,N',N'-tetraphenylis used in environmental and health risk assessments to evaluate its impact and develop appropriate safety measures for its use and handling.

Check Digit Verification of cas no

The CAS Registry Mumber 279672-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,9,6,7 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 279672-22:
(8*2)+(7*7)+(6*9)+(5*6)+(4*7)+(3*2)+(2*2)+(1*2)=189
189 % 10 = 9
So 279672-22-9 is a valid CAS Registry Number.

279672-22-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-N,6-N,12-N,12-N-tetraphenylchrysene-6,12-diamine

1.2 Other means of identification

Product number -
Other names 6,12-Chrysenediamine,N,N,N',N'-tetraphenyl

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:279672-22-9 SDS

279672-22-9Downstream Products

279672-22-9Relevant academic research and scientific papers

Highly efficient emitters of ultra-deep-blue light made from chrysene chromophores

Shin, Hwangyu,Jung, Hyocheol,Kim, Beomjin,Lee, Jaehyun,Moon, Jiwon,Kim, Joonghan,Park, Jongwook

, p. 3833 - 3842 (2016)

Chrysene, which has a wide band gap, was selected as an emission core to develop and study new materials that emit ultra-deep-blue light with high efficiency. Six compounds introducing various side groups were designed and synthesized: 6,12-bis(3′,5′-diph

Substitution effect of super hydrophobic units: A new strategy to design deep blue fluorescent emitters

Li, Ke,Yang, Shuai,Murtaza, Imran,Liu, Ming,He, Gufeng,Chen, Yantong,He, Yaowu,Goto, Osamu,Shen, Clifton,Meng, Hong

, p. 747 - 755 (2017)

Fluorescent deep-blue emitters consisting of arylamine chrysene have attracted immense commercial interest in organic light-emitting devices (OLEDs). Herein, we endeavor to design emitters with super hydrophobic groups, namely trifluoromethoxy ([sbnd]OCF

Diboron fluorescent material as well as preparation method and device thereof OLED

-

Paragraph 0056-0057, (2019/12/08)

The invention discloses a double-boron fluorescent material, a preparation method thereof and an OLED (organic light-emitting diode) device. A molecular structure general formula of the material is shown in the description, wherein Ar is an aromatic ring

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