25032-74-0

Usage

Uses

Used in Organic Synthesis:
3,3'-Dibromobenzophenone is used as a building block for the synthesis of more complex organic compounds, contributing to the development of new pharmaceuticals, agrochemicals, and other fine chemicals.
Used in Pharmaceutical Production:
3,3'-Dibromobenzophenone is used as a starting material in the production of various pharmaceuticals, enabling the creation of new and effective medications.
Used in Agrochemical Production:
3,3'-Dibromobenzophenone is utilized as a starting material in the synthesis of agrochemicals, aiding in the development of innovative and efficient crop protection products.
Used in Polymer Material Production:
3,3'-Dibromobenzophenone is used as a photoinitiator in the production of polymer materials, such as coatings, adhesives, and sealants, enhancing their properties and performance.
Used in Optical and Electronic Material Manufacturing:
3,3'-Dibromobenzophenone is employed in the manufacture of optical and electronic materials, contributing to the advancement of technology in these fields.

Upstream product

• 119-61-9 benzophenone 
• 6952-59-6 3-cyanobromobenzene 
• 108-36-1 1,3-dibromobenzene 
• 7732-18-5 water 
• 7726-95-6 bromine 
• 7553-56-2 iodine 
• 51339-30-1 3,3'-dibromophenylmethanol 
• 3132-99-8 m-bromobenzoic aldehyde 
• 2592-86-1 (m-Bromophenyl)lithium 
• 79-44-7 N,N-Dimethylcarbamoyl chloride 
• 105-58-8 Diethyl carbonate 
• 591-18-4 1-Bromo-3-iodobenzene 
• 24398-88-7 ethyl 3-bromobenzoate 

Downstream Products

• 69754-48-9 3-bromo-benzoic acid-(3-bromo-anilide) 
• 51339-30-1 3,3'-dibromophenylmethanol 
• 130249-08-0 3,3'-Bis<(trimethylsilyl)ethinyl>benzophenon 
• 130201-37-5 2,2-Bis(3-bromphenyl)-1,3-dioxan 
• 29265-85-8 1,1-bis(3-bromophenyl)ethene 
• 859315-37-0 1-bromo-4-(1-(4-bromophenyl)-2,2-diphenylvinyl)benzene 
• 263249-05-4 bis(3-bromophenyl)difluoromethane 
• 1211547-22-6 9,9-bis(3-bromophenyl)-9H-fluorene 
• 1270278-03-9 9,9-bis-(3-hydroxymethylphenyl)-9H-fluorene 
• 1270278-04-0 9,9-bis(3-chloromethylphenyl)-9H-fluorene 
• 1569852-62-5 C₃₈H₄₂B₂O₄ 
• 1569852-68-1 C₆₂H₄₆N₂ 
• 1569852-74-9 C₆₂H₄₆N₂ 
• 1569852-71-6 C₆₂H₄₆N₂ 

Relevant academic research and scientific papers

A donor-acceptor-type host material for solution-processed phosphorescent organic light-emitting devices showing high efficiency

The solution-processable host material, 3,3′-[bis(9-phenyl-carbazol-3-yl)]benzophenone (BCzBP), containing donor-type phenylcarbazole units and an acceptor-type benzophenone unit was synthesized. BCzBP showed a high excited triplet energy level and a high

Aggregation-Induced-Emission-Active Macrocycle Exhibiting Analogous Triply and Singly Twisted M?bius Topologies

Molecules with M?bius topology have drawn increasing attention from scientists in a variety of fields, such as organic chemistry, inorganic chemistry, and material science. However, synthetic difficulties and the lack of functionality impede their fundame

Fused ring compound as well as preparation method and application thereof as well as CO-host material Light-emitting composition, light-emitting device, lighting apparatus, and display apparatus

Disclosed are fused ring compounds having a structure represented by Formula 1 or Formula 2, a method for preparing the same, a co-host material containing the condensed cyclic compound, a light emitting composition, a light emitting device and containing

Method for preparing symmetric diarylketone through catalytic oxidative carbonylation

The invention discloses a method for preparing symmetric diarylketone of a formula (I) as shown in the description. The method comprises the following steps: mixing arylboronic acid (II) (Ar-B(OH)2 (II)), a palladium catalyst, a promoter and an organic solvent in a reactor, introducing air and CO having a volume ratio of (7-19):1, reacting under the conditions of a pressure of 1-6 atm and a temperature of 30-80 DEG C for 8-16 hours, and performing after-treatment on the reaction solution, thereby obtaining the product symmetric diarylketone. According to the method disclosed by the invention,the air directly serves as an oxidizing agent to replace the O2 to be applied to oxidative carbonylation of the arylboronic acid, and the ratio of the air to CO is beyond an explosion limit. Therefore, the catalytic system is safe and economic. The palladium catalyst is small in dosage and simple in separation and can be recycled for several times. The method disclosed by the invention is mild inreaction condition, excellent in substrate suitability and high in yield.

Organic metal compounds and organic light emitting diodes comprising the same

PURPOSE: An organic metal compound and an organic electroluminescent device containing the same are provided to ensure excellent thermal property and luminescence efficiency, and to be used in a display and a light. CONSTITUTION: An organic metal compound contains a compound of chemical formula 1. An organic electroluminescent device contains the organic metal compound of chemical formula 1. The compound is contained in a light emitting layer between anode and cathode. The organic electroluminescent device comprises one or more layers selected from a hole injection layer, a hole transport layer, an electron blocking layer, a hole blocking layer, an electron transport layer, and an electron injection layer between the anode and the cathode.

COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present invention provides a compound represented by chemical formula 1, and an organic light emitting device comprising the same. The compound of the present invention can be used as a material of an organic material layer of an organic light emitting device, and can improve the efficiency, low driving voltage and/or the lifetime characteristic in the organic light emitting device.COPYRIGHT KIPO 2018

COMPOUND AND ORGANIC LIGHT EMITTING DEVICE COMPRISING THE SAME

The present specification provides a compound represented by chemical formula 1, and an organic light emitting device comprising the same. The compound of the present specification can be used as a material of an organic material layer of an organic light emitting device, and can improve the efficiency, low driving voltage and/or the lifetime characteristic in the organic light emitting device.COPYRIGHT KIPO 2018

Substituted carbazole diphenyl ketone compound and an organic electroluminescence element

PROBLEM TO BE SOLVED: To provide a novel compound which is a low-molecular material having both of sufficiently high excitation triplet energy and a charge injection-transport property, which is scarcely soluble in an alcoholic solvent, and with which a f

Importance of the Anchor Group Position (Para versus Meta) in Tetraphenylmethane Tripods: Synthesis and Self-Assembly Features

The efficient synthesis of tripodal platforms based on tetraphenylmethane with three acetyl-protected thiol groups in either meta or para positions relative to the central sp3carbon for deposition on Au (111) surfaces is reported. These platfor

MATERIALS FOR ELECTRONIC DEVICES

The present invention relates to a compound, comprising a pyrene skeleton and arylamino groups, according to formula (I). The compound is suitable for use as a functional material in electronic devices.