332083-45-1

Basic information

• Product Name: 9,10-dibroMo-2,6-di-tert-butylanthracene
• Synonyms: 9,10-dibroMo-2,6-di-tert-butylanthracene;9,10-dibromo-2,6-di-tert-butylanthracene ada@tuskwei.com sky
• CAS NO: 332083-45-1
• Molecular Formula: C₂₂H₂₄Br₂
• Molecular Weight: 448.23396
• Mol File: 332083-45-1.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 9,10-dibroMo-2,6-di-tert-butylanthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 9,10-dibroMo-2,6-di-tert-butylanthracene(332083-45-1)
• EPA Substance Registry System: 9,10-dibroMo-2,6-di-tert-butylanthracene(332083-45-1)

Safety Data

• Hazardous Substances Data: 332083-45-1(Hazardous Substances Data)

Usage

General Description

9,10-dibromo-2,6-di-tert-butylanthracene is a powerful and versatile chemical compound known for its use as a reactive intermediate in organic synthesis. 9,10-dibroMo-2,6-di-tert-butylanthracene is a substituted anthracene derivative with two bromine atoms at the 9th and 10th positions, and two tert-butyl groups at the 2nd and 6th positions. It is commonly used as a reagent in chemical reactions to introduce functional groups into organic molecules, and it also serves as a valuable building block in the synthesis of various materials and pharmaceuticals. Its highly reactive nature and unique molecular structure make it a valuable tool in the field of organic chemistry for the creation of novel compounds and materials.

Upstream product

• 120-12-7 anthracene 
• 62375-58-0 2,6-di-tert-butylanthracene 
• 99964-58-6 2,7-di-tert-butylanthracene 

Downstream Products

• 1309922-55-1 (E)-2-cyano-3-(5-(7-(5-(2,6-di-tert-butyl-10-(naphthalen-1-yl(phenyl)amino)anthracen-9-yl)thiophen-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)thiophen-2-yl)acrylic acid 
• 1309922-60-8 5-(7-(5-(2,6-di-tert-butyl-10-(naphthalen-1-yl(phenyl)amino)anthracen-9-yl)thiophen-2-yl)benzo[c][1,2,5]thiadiazol-4-yl)thiophene-2-carbaldehyde 
• 1309922-59-5 5'-(2,6-di-tert-butyl-10-(naphthalen-1-yl(phenyl)amino)anthracen-9-yl)-2,2'-bithiophene-5-carbaldehyde 
• 1309922-53-9 (E)-2-cyano-3-(5-(2,6-di-tert-butyl-10-(naphthalen-1-yl(phenyl)amino)anthracen-9-yl)thiophen-2-yl)acrylic acid 
• 1309922-58-4 5-(2,6-di-tert-butyl-10-(naphthalen-1-yl(phenyl)amino)anthracen-9-yl)thiophene-2-carbaldehyde 
• 1309922-57-3 2,6-di-tert-butyl-N-(naphthalen-1-yl)-N-phenyl-10-(thiophen-2-yl)anthracen-9-amine 
• 1309459-79-7 C₇₄H₆₀N₆O₂ 
• 519171-70-1 9,10-bis[4-(2,2-diphenylethenyl)phenyl]-2,7-di-t-butylanthracene 
• 519171-69-8 9,10-bis[4-(2,2-diphenylethenyl)phenyl]-2,6-di-t-butylanthracene 
• 1092110-07-0 C₄₆H₃₆F₈N₂ 

Relevant articles and documents

Solvent-assisted synthesis of a shape-persistent chiral polyaza gigantocycle characterized by a very large internal cavity and extraordinarily high amplitude of the ECD exciton couplet

A giant, chiral square-shaped octaimine macrocycle has been obtained in a controlled manner from readily available and inexpensive substrates: 9,10-diphenylanthracene-based dialdehyde and trans-1,2-diaminocyclohexane. Reduction of the polyimine led to a c

Organic luminous material based on anthracene and derivative of anthracene, preparation method and application of organic luminous material

The invention belongs to the technical field of organic luminous materials and discloses an organic luminous material based on anthracene and a derivative of anthracene, and a preparation method and application of the organic luminous material. A structural formula of the organic luminous material based on anthracene and the derivative of anthracene is shown as formula I as shown in the specification; R1, R2, R3 and R4 are hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl and substituted or unsubstituted aryl or heteroaryl independently; R1 and R2 are substituted or unsubstituted aryl or heteroaryl preferably; and R3 and R4 are alkyl preferably. The invention further discloses the preparation method of the luminous material. The organic luminous materialhas the characteristics of adjustable spectrum, high quantum yield, good heat stability and the like and has a high potential application value in the fields of organic light emitting diodes, organicfield effect transistors, organic solar batteries, fluorescent sensors, biological detection and the like.

C-9 fluorenyl substituted anthracenes: A promising new family of blue luminescent materials

Syntheses, optical, and electrochemical properties of novel C-9 fluorenyl substituted anthracenes linked by a tetrahedral sp3-hybridized carbon atom are reported for blue light emitting materials. Remarkably, an unoptimized organic light-emitting diode based on 1-fold fluorene-functionalized anthracene 3 exhibits a radiance of 4100 cd/m2 at 12 V and a maximum EL efficiency of 1.36 cd/A with color purity CIE x, y (0.157, 0.082), which is very close to the National Television System Committee standard blue.