114583-08-3

Basic information

• Product Name: 2-TERTBUTYL-9,10-DIBROMOANTHRACENE
• Synonyms: 2-TERTBUTYL-9,10-DIBROMOANTHRACENE;9,10-dibromo-2-(tert-butyl)anthracene
• CAS NO: 114583-08-3
• Molecular Formula: C₁₈H₁₆Br₂
• Molecular Weight: 392.13
• EINECS: 200-258-5
• Mol File: 114583-08-3.mol

Chemical Properties

• Boiling Point: 456.1°Cat760mmHg
• Flash Point: 268.2°C
• Appearance: /
• Density: 1.527g/cm³
• Vapor Pressure: 4.49E-08mmHg at 25°C
• Refractive Index: 1.668
• CAS DataBase Reference: 2-TERTBUTYL-9,10-DIBROMOANTHRACENE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-TERTBUTYL-9,10-DIBROMOANTHRACENE(114583-08-3)
• EPA Substance Registry System: 2-TERTBUTYL-9,10-DIBROMOANTHRACENE(114583-08-3)

Safety Data

• Hazardous Substances Data: 114583-08-3(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
2-TERTBUTYL-9,10-DIBROMOANTHRACENE is used as a building block in organic synthesis for the creation of complex organic compounds. Its unique structure and reactivity make it a valuable component in the synthesis of various organic molecules.
Used in Materials Science:
In the field of materials science, 2-TERTBUTYL-9,10-DIBROMOANTHRACENE is used as a precursor for the development of new materials with specific properties. Its thermal stability and chemical structure contribute to the creation of materials with potential applications in various industries.
Used in Medicinal Chemistry:
2-TERTBUTYL-9,10-DIBROMOANTHRACENE is utilized in medicinal chemistry for the synthesis of pharmaceutical compounds. Its chemical properties allow for the development of new drugs with potential therapeutic effects.
Used in the Production of Dyes and Pigments:
2-TERTBUTYL-9,10-DIBROMOANTHRACENE is used as a starting material in the production of various dyes and pigments. Its chemical structure contributes to the color and stability of these products, making it a valuable component in the dye and pigment industry.
Used in Pharmaceutical Production:
2-TERTBUTYL-9,10-DIBROMOANTHRACENE is used in the production of pharmaceuticals, where its unique properties can be leveraged to create new drugs with specific therapeutic effects.

InChI:InChI=1/C18H16Br2/c1-18(2,3)11-8-9-14-15(10-11)17(20)13-7-5-4-6-12(13)16(14)19/h4-10H,1-3H3

Upstream product

• 18801-00-8 2-(t-butyl)anthracene 

Downstream Products

• 274905-73-6 2-tert-butyl-9,10-bis-(β-naphthyl)-anthracene 
• 250339-07-2 2-tert-butyl-9,10-bis(2-biphenyl)anthracene 

Relevant articles and documents

The anthracene derivatives, organic EL material and its manufacturing method (by machine translation)

PROBLEM TO BE SOLVED: To provide an anthracene derivative in which a specific solubility radical is introduced into an anthracene skeleton, thereby improving solubility, and that is suitable to be used for film production in a solution process, and further to provide an anthracene derivative in which a specific solution radical of the anthracene derivative is desorbed by an external stimulation, and that is as an organic EL material excellent in characteristics.SOLUTION: For instance, anthracene derivatives (HTL1) and (HTL2) are exemplified to be synthesized by reaction formula (A). The anthracene derivative excellent in organic EL characteristics is obtained by the desorption of an ester group by an external stimulation.

High-color-purity and high-efficiency non-doped deep-blue electroluminescent devices based on novel anthracene derivatives

Two novel anthracene derivatives 2-tert-butyl-9,10-bis(2-biphenyl) anthracene (TBBPA) and 2-tert-butyl-9,10-bis[2-(1-naphthyl)phenyl]anthracene (TBNPA) were synthesized and characterized. The quantum chemical calculations show that TBBPA and TBNPA have hi

RELATIVE YIELDS OF EXCITED KETONES FROM SELF-REACTIONS OF ALKOXYL AND ALKYLPEROXYL RADICAL PAIRS

We have measured the ratios of excited ketones that arise from the self-reactions of alkoxyl (2R1R2CHO.) and peroxyl (2R1R2CHO. radicals.This was accomplished by measuring the chemiluminescence emission from solutions of R1R2CHO2H, or R1R2CH2 and O2, in the presence of a free-radical initiator trans-RON=NOR, in which R=t-Bu or R1R2CH in paired experiments.The excited states were trapped with 2-tert-butyl-9,10-dibromoanthracene or another fluorescent derivative of anthracene.The peroxyls were less efficient sources by 17percent, 48percent, and 42percent than the alkoxyls for the cases in which R1R2C=O was acetophenone in ethylbenzene, cyclohexanone in cyclohexane, and 1-tetralone in t-BuPh and in t-BuOH, respectively.The activation energy for formation of excited 1-tetralone (To and/or S1) from two 1-tetralylperoxyl radicals was 6 +/- 3 kcal/mol higher than for production of excited state from the corresponding pair of alkoxyl radicals.The results are consistent with but do not demand the hypotesis that excited carbonyl states arise in peroxyl terminations by way of alkoxyl pairs.