1065644-53-2

Basic information

• Product Name: 2,6-DibroMo-9,10-dihydroanthracene
• Synonyms: 2,6-DibroMo-9,10-dihydroanthracene
• CAS NO: 1065644-53-2
• Molecular Formula: C14H10Br2
• Molecular Weight: 338.0372
• Mol File: 1065644-53-2.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 378.1±42.0 °C(Predicted)
• Appearance: /
• Density: 1.703±0.06 g/cm3(Predicted)
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 2,6-DibroMo-9,10-dihydroanthracene(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-DibroMo-9,10-dihydroanthracene(1065644-53-2)
• EPA Substance Registry System: 2,6-DibroMo-9,10-dihydroanthracene(1065644-53-2)

Safety Data

• Hazardous Substances Data: 1065644-53-2(Hazardous Substances Data)

Usage

Description

2,6-Dibromo-9,10-dihydroanthracene, with the molecular formula C14H12Br2, is a chemical compound derived from anthracene, a polycyclic aromatic hydrocarbon. It is characterized by the presence of two bromine atoms at the 2nd and 6th positions and a dihydro structure at the 9th and 10th positions. This yellowish solid is insoluble in water but readily soluble in organic solvents. Due to its potential hazards, it requires careful handling.

Uses

Used in Organic Synthesis:
2,6-Dibromo-9,10-dihydroanthracene is utilized as a key intermediate in organic synthesis for the production of various organic compounds. Its unique structure allows for versatile chemical reactions, making it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in the Production of Larger Organic Molecules:
As a derivative of anthracene, 2,6-Dibromo-9,10-dihydroanthracene serves as a fundamental component in the assembly of larger and more complex organic molecules. Its bromine atoms facilitate coupling reactions, enabling the formation of extended π-conjugated systems and other structural motifs that are essential in materials science and medicinal chemistry.
Used in Chemical Research:
2,6-Dibromo-9,10-dihydroanthracene is also employed in chemical research as a model compound for studying reaction mechanisms, exploring the properties of polycyclic aromatic hydrocarbons, and developing new synthetic methodologies. Its reactivity and structural features provide insights into the behavior of similar compounds and contribute to the advancement of organic chemistry.