105836-96-2

Basic information

• Product Name: 2,8-dibromooxanthrene
• Synonyms: 2,8-dibromooxanthrene;2,8-DIBROMODIBENZO-PARA-DIOXIN
• CAS NO: 105836-96-2
• Molecular Formula: C₁₂H₆Br₂O₂
• Molecular Weight: 0
• Mol File: 105836-96-2.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 376.6°Cat760mmHg
• Flash Point: 154.5°C
• Appearance: /
• Density: 1.894g/cm³
• Vapor Pressure: 1.55E-05mmHg at 25°C
• Refractive Index: 1.674
• CAS DataBase Reference: 2,8-dibromooxanthrene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,8-dibromooxanthrene(105836-96-2)
• EPA Substance Registry System: 2,8-dibromooxanthrene(105836-96-2)

Safety Data

• Hazardous Substances Data: 105836-96-2(Hazardous Substances Data)

Usage

Appearance

Brightly colored yellow solid 2,8-dibromooxanthrene has a vivid yellow color and is a solid at room temperature.

Usage

Manufacturing of dyes and pigments This compound is utilized in the production of various dyes and pigments for different industries.

Chemical family

Xanthene 2,8-dibromooxanthrene belongs to the xanthene family, which is a group of organic compounds.

Derivation

Substitution of two bromine atoms at the 2 and 8 positions This compound is derived from xanthene by replacing two hydrogen atoms with bromine atoms at specific positions on the molecule.

Hazardous nature

Potential health and environmental risks 2,8-dibromooxanthrene is considered hazardous, and proper handling precautions should be taken to minimize exposure and environmental contamination.

Stability

High heat and light stability This compound is known for its ability to withstand high temperatures and resist degradation from exposure to light, making it suitable for various industrial applications.

Industrial applications

Textile and paper production Due to its stability, 2,8-dibromooxanthrene is used in industries such as textile and paper production to provide color and stability to the final products.

InChI:InChI=1/C12H6Br2O2/c13-7-1-3-9-11(5-7)16-12-6-8(14)2-4-10(12)15-9/h1-6H

Upstream product

• 262-12-4 dioxin 
• 1354655-73-4 C₁₂H₇Br₂NO₄ 
• 1354655-72-3 C₁₃H₉Br₂NO₄ 
• 364-73-8 4-Bromo-1-fluoro-2-nitrobenzene 
• 37942-01-1 5-bromo-2-methoxyphenol 
• 139458-06-3 2-trimethylsilyldibenzo<1,4>dioxin 
• 95-50-1 1,2-dichloro-benzene 
• 120-80-9 benzene-1,2-diol 

Downstream Products

• 109333-32-6 2,8-dibromo-3,7-dichlorodibenzo-p-dioxin 

Relevant articles and documents

Discovery of fused tricyclic core containing HCV NS5A inhibitors with pan-genotype activity

HCV NS5A inhibitors have demonstrated impressive in vitro potency profiles in HCV replicon assays and robust HCV RNA titer reduction in the clinic making them attractive components for inclusion in an all oral fixed dose combination regimen for the treatment of HCV infection. Herein, we describe research efforts that led to the discovery of a series of fused tricyclic core containing HCV NS5A inhibitors such as 24, 39, 40, 43, and 44 which have pan-genotype activity and are orally bioavailable in the rat.

ORDER OF THE REPLACEMENT OF HYDROGEN BY HALOGEN IN THE HALOGENATION OF DIBENZO-p-DIOXIN AND ITS NITRO AND AMINO DERIVATIVES

The order of the replacement of hydrogen by halogen in the bromination and chlorination of dibenzo-p-dioxin and its nitro and amino derivatives was examined with the purpose of determining the possibilities of the formation of highly toxic isomers of halogenated dibenzo-p-dioxins from precursors with a tricyclic structure of dibenzo-p-dioxin.A number of halogenated dibenzo-p-dioxins were synthesized, which illustrates the order of the replacement, and their physicochemical and spectral characteristics are given.

EFFECT OF THE CROWN ETHER 18-CROWN-6-ON CHLORINATION OF DIBENZO-p-DIOXIN AND ITS DERIVATIVES

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