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2,7-dibromo-4,5-diazafluoren-9-one is a complex chemical compound that belongs to the fluorene family of chemicals. It is characterized by the presence of two bromine atoms, as indicated by 'dibromo,' nitrogen atoms ('diaza'), and an oxygen atom ('one' end). The fluorene family is known for its polycyclic aromatic hydrocarbon structure, which consists of fused benzene rings. The specific properties, uses, and toxicity of 2,7-dibromo-4,5-diazafluoren-9-one cannot be determined solely from its name and would require further experimental data or context within the chemical research or industry.

77213-41-3

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77213-41-3 Usage

Uses

Used in Chemical Research:
2,7-dibromo-4,5-diazafluoren-9-one is used as a research compound for studying its chemical properties and potential applications in various fields. Its unique structure with bromine and nitrogen atoms may offer insights into new chemical reactions or synthesis pathways.
Used in Pharmaceutical Industry:
2,7-dibromo-4,5-diazafluoren-9-one is used as a potential pharmaceutical intermediate for the development of new drugs. Its structure may provide a basis for designing molecules with specific therapeutic properties, such as antimicrobial, anticancer, or antiviral activities.
Used in Material Science:
2,7-dibromo-4,5-diazafluoren-9-one is used as a building block in the synthesis of advanced materials, such as organic semiconductors or polymers with unique electronic, optical, or mechanical properties. Its incorporation into these materials may lead to the development of new technologies in electronics, energy storage, or sensing applications.
Used in Environmental Applications:
2,7-dibromo-4,5-diazafluoren-9-one may be used as a component in the development of environmental remediation technologies, such as adsorbents for the removal of pollutants from water or air. Its chemical structure could potentially interact with contaminants, facilitating their capture and separation from the environment.

Check Digit Verification of cas no

The CAS Registry Mumber 77213-41-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,2,1 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 77213-41:
(7*7)+(6*7)+(5*2)+(4*1)+(3*3)+(2*4)+(1*1)=123
123 % 10 = 3
So 77213-41-3 is a valid CAS Registry Number.

77213-41-3Downstream Products

77213-41-3Relevant academic research and scientific papers

Nitrogen-containing organic compound, application thereof and organic light-emitting device

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Paragraph 0156; 0157; 0158, (2020/08/30)

The invention relates to the field of organic light-emitting devices, and discloses a nitrogen-containing organic compound, application thereof and an organic light-emitting device. The nitrogen-containing organic compound has a structure as shown in a fo

Organic electroluminescent compound, applications thereof, and organic electroluminescent device

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Paragraph 0067-0069, (2020/03/17)

The invention relates to the field of o organic electroluminescent devices and discloses an organic electroluminescent compound, applications thereof, and an organic electroluminescent device. The compound has the structure shown as the formula (I), where

Facile synthesis and self-assembly of diazafluorenone-based p-n (donor-acceptor) organic semiconductors

Li, Wei-Jie,Wu, Hai-Mei,Li, Yi-Bao,Hu, Chao-Peng,Yi, Ming-Dong,Xie, Ling-Hai,Chen, Lin,Zhao, Jian-Feng,Zhao, Xiang-Hua,Shi, Nai-En,Qian, Yan,Wang, Chen,Wei, Wei,Huang, Wei

experimental part, p. 8216 - 8221 (2012/09/22)

A mild and effective method to prepare 2,7-dibromo-4,5-diazafluoren-9-one (3) has been described involving tandem oxidation and rearrangement reactions. Diazafluorenone-based donor-acceptor (p-n) molecules via stille coupling reactions exhibit solvent-dep

Electrophilic Substitution in the Azafluorenone Systems - Bromination of Azafluorenones

Mlochowski, Jacek,Szulc, Zdzislaw

, p. 971 - 980 (2007/10/02)

Die Bromierung von 1- und 4-Aza- und 1,5-, 1,8- und 4,5-Diazafluorenonen 1-5 mit N-Bromsuccinimid, Brom in Schwefelsaeure oder mit Brom 60proz.Oleum wurde als Modellreaktion fuer die elektrophile Substitution in Azafluorenon-Systemen untersucht.Die Bromierung von Monoazafluorenonen mit N-Bromsuccinimid in Schwefelsaeure und Diazafluorenonen mit Brom in 60proz.Oleum ist eine guenstige Methode zur Darstellung von bisher unbekannten Bromazafluorenonen.Die Strukturen der erhaltenen Bromderivate wurden mit Hilfe der 1H-NMR-Spektroskopie festgestellt.Die Ergebnisse der Substitution wurden in Abhaengigkeit von der elektronischen Struktur der Azafluorenon-Systeme diskutiert.

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