118599-27-2

Basic information

• Product Name: 9-Benzyl-3,6-dibroMocarbazole
• Synonyms: 9-Benzyl-3,6-dibroMocarbazole
• CAS NO: 118599-27-2
• Molecular Formula: C₁₉H₁₃Br₂N
• Molecular Weight: 415.12122
• Mol File: 118599-27-2.mol
• Article Data: 17

Chemical Properties

• Melting Point: 160.0 to 164.0 °C
• Appearance: /
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: 9-Benzyl-3,6-dibroMocarbazole(CAS DataBase Reference)
• NIST Chemistry Reference: 9-Benzyl-3,6-dibroMocarbazole(118599-27-2)
• EPA Substance Registry System: 9-Benzyl-3,6-dibroMocarbazole(118599-27-2)

Safety Data

• Hazardous Substances Data: 118599-27-2(Hazardous Substances Data)

Usage

Description

9-Benzyl-3,6-dibromocarbazole is a chemical compound belonging to the carbazole family. It is a dibrominated derivative of benzylcarbazole, featuring two bromine atoms attached to the 3 and 6 positions of the carbazole ring. 9-Benzyl-3,6-dibroMocarbazole is known for its unique reactivity and properties due to the presence of bromine atoms, making it a valuable component in various chemical processes and applications.

Uses

Used in Organic Synthesis:
9-Benzyl-3,6-dibromocarbazole is utilized as a building block in organic synthesis for the production of various organic compounds and materials. Its unique reactivity and properties contribute to the creation of a wide range of chemical products.
Used in Organic Electronics:
In the field of organic electronics, 9-Benzyl-3,6-dibromocarbazole is employed for its potential applications, likely due to its electronic properties and the ability to form complexes or compounds that can be used in electronic devices or materials.
Used in Pharmaceutical Synthesis:
9-Benzyl-3,6-dibromocarbazole is also used as a starting material or intermediate in the synthesis of pharmaceuticals. Its unique structure and reactivity can be leveraged to develop new drugs with specific therapeutic properties.
Used in Agrochemical Production:
Furthermore, this compound finds application in the synthesis of agrochemicals, where it may be used to create pesticides, herbicides, or other agricultural chemicals that can enhance crop protection and yield.

Upstream product

• 6825-20-3 3,6-dibromo-9H-carbazole 
• 100-44-7 benzyl chloride 
• 19402-87-0 9-benzyl-9H-carbazole 
• 86-74-8 9H-carbazole 
• 100-39-0 benzyl bromide 
• 100-51-6 benzyl alcohol 
• 79990-92-4 3,6-dibromocarbazole nitranion 

Downstream Products

• 1357174-27-6 4,4'-(9-benzyl-9H-carbazole-3,6-diyl)dibenzaldehyde 
• 1630723-98-6 N³,N³,N⁶,N⁶-tetrakis(4-methoxyphenyl)-9-H-carbazole-3,6-diamine 
• 797057-71-7 9-benzyl-3,6-di(9-carbazolyl)-9H-carbazole 
• 1222558-44-2 9-benzyl-3,6-bis-triisopropylsilanyl-9H-carbazole 
• 1033781-67-7 N-benzyl-3,6-bis[3,6-bis(9,9'-di-n-propylfluoren-2-yl)carbazol-9-yl]carbazole 
• 937255-41-9 3,6-diethynyl-9-benzylcarbazole 

Relevant articles and documents

Diazadioxa[8]circulenes: Planar antiaromatic cyclooctatetraenes

In this paper we describe a new class of antiaromatic planar cyclooctatetraenes: the diazadioxa[8]circulenes. The synthesis was achieved by means of a new acid-mediated oxidative dimerization of 3,6-dihydroxycarbazoles to yield the diazadioxa[8]circulenes

Branched Methoxydiphenylamine-Substituted Carbazole Derivatives for Efficient Perovskite Solar Cells: Bigger Is Not Always Better

A set of novel branched molecules bearing a different number of 3,6-bis(4,4′-dimethoxydiphenylamino)carbazole-based (Cz-OMeDPA) periphery arms linked together by aliphatic chains have been developed, and their performance has been tested in perovskite sol

Polymer-Supported Cation Radicals

Reaction of chloromethylated polystyrene (3.90 mequiv/g) beads with triphenylamine and diethylchloroalane resulted in a higly cross-linked polymer.The chloromethylated polystyrene was modified by reaction with 2,6-dibromocarbazole (4) and K2CO3 in DMF at 100 deg C to give an excellent yield of polymer-supported 2,6-dibromocarbazole (5) without concomitant cross-linking.The polymer-bound 2,6-dibromocarbazole was nonreactive toward SbCl5, whereas the homogeneous counterpart 9-N-benzyl-2,6-dibromocarbazole (6) was found to readily generate the aminium cation radical upon reaction with SbCl5.Attachment of phenothiazine to a polystyrene support yielded a reagent that would react very rapidly with SbCl5 in dichloromethane.The polymer-bound phenothiazine cation radical was found to readily oxidize the metal-metal bond in 2 and undergo anion exchange with Bu4NPF6 to afford a more synthetically useful reagent.

Carbazole-nitrogen heterocyclic A-D-A type room-temperature organic phosphorescent white light material

The invention belongs to the field of organic luminescent materials, and particularly relates to a carbazole-nitrogen heterocyclic A-D-A type room-temperature organic phosphorescent white light material. The room-temperature organic phosphorescent white l

A benzhydryl radical based on the room temperature of the organic light-emitting material and using the material preparation of organic electroluminescent device

A benzhydryl radical based on the stability of the organic light-emitting material at room temperature and using the material preparation of the organic electroluminescent device, which belongs to the field of organic light-emitting technology. The present invention in the preparation of the organic light-emitting material, the center of the common characteristic is the carbon free radical, is composed of two C - C covalent bond and a C - N to form a covalent bond. Stability is the light-emitting free radical material in the application of the key nature, connected to the electronic group conducive to stable free radical, in this invention through the nitrogen-containing heterocyclic carbazole, indole, dimethyl acridine and the like in the electronic group to the nitrogen atom is connected directly to the benzyl group, to obtain a stable benzhydryl radical, its stability and PTM, compared with the TTM is greatly improved, and has a room temperature fluorescent. The preparation of the material of the organic electroluminescent device using double thread condition exciton light-emitting, can avoid the traditional organic electroluminescent device in the use of the triplet state exciton, the maximum external quantum efficiency of the device is 0.66%.