Welcome to LookChem.com Sign In|Join Free


  • or


Post Buying Request

118599-27-2 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

118599-27-2 Usage

General Description

9-Benzyl-3,6-dibromocarbazole is a chemical compound that belongs to the carbazole family. It is a dibrominated derivative of benzylcarbazole, with two bromine atoms attached to the 3 and 6 positions of the carbazole ring. 9-Benzyl-3,6-dibroMocarbazole is often used in organic synthesis and as a building block for the production of various organic compounds and materials. It has been studied for its potential applications in the field of organic electronics, as well as in the synthesis of pharmaceuticals and agrochemicals. The presence of bromine atoms in its structure gives 9-Benzyl-3,6-dibromocarbazole unique reactivity and properties, making it a valuable compound for various chemical processes and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 118599-27-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,5,9 and 9 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 118599-27:
162 % 10 = 2
So 118599-27-2 is a valid CAS Registry Number.

118599-27-2 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail
  • TCI America

  • (B4348)  9-Benzyl-3,6-dibromocarbazole  >98.0%(GC)(N)

  • 118599-27-2

  • 1g

  • 995.00CNY

  • Detail



According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017


1.1 GHS Product identifier

Product name 9-Benzyl-3,6-dibromocarbazole

1.2 Other means of identification

Product number -
Other names 9-benzyl-3,6-dibromocarbazole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:118599-27-2 SDS

118599-27-2Relevant articles and documents

Diazadioxa[8]circulenes: Planar antiaromatic cyclooctatetraenes

Hensel, Thomas,Trpcevski, Denis,Lind, Christopher,Grosjean, Remi,Hammershoj, Peter,Nielsen, Christian B.,Brock-Nannestad, Theis,Nielsen, Bjarne E.,Schau-Magnussen, Magnus,Minaev, Boris,Baryshnikov, Gleb V.,Pittelkow, Michael

, p. 17097 - 17102 (2013)

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

Luizys, Povilas,Xia, Jianxing,Daskeviciene, Maryte,Kantminiene, Kristina,Kasparavicius, Ernestas,Kanda, Hiroyuki,Zhang, Yi,Jankauskas, Vygintas,Rakstys, Kasparas,Getautis, Vytautas,Nazeeruddin, Mohammad Khaja

, p. 7017 - 7027 (2021)

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

Wright, Michael E.,Jin, Myung-Jong

, p. 965 - 968 (1989)

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


Paragraph 0026-0030, (2021/02/10)

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


Paragraph 0063; 0074; 0075, (2018/07/30)

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%.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)


What can I do for you?
Get Best Price

Get Best Price for 118599-27-2