27973-29-1

  • Product Name:1,6-dibromopyrene
  • Molecular Formula:C16H8Br2
  • Purity:99%
  • Molecular Weight:360.048
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Product Details

pd_meltingpoint:228.0 to 232.0 °C

Appearance:White to off-white powder

Purity:99%

High quality purity >99% 1,6-dibromopyrene 27973-29-1 for sale

  • Molecular Formula:C16H8Br2
  • Molecular Weight:360.048
  • Appearance/Colour:White to off-white powder 
  • Vapor Pressure:1.54E-08mmHg at 25°C 
  • Melting Point:228.0 to 232.0 °C 
  • Refractive Index:1.863 
  • Boiling Point:469.6 °C at 760 mmHg 
  • Flash Point:277.3 °C 
  • PSA:0.00000 
  • Density:1.852 g/cm3 
  • LogP:6.10900 

1,6-Dibromopyrene(Cas 27973-29-1) Usage

InChI:InChI=1/C16H8Br2/c17-13-8-4-10-2-6-12-14(18)7-3-9-1-5-11(13)16(10)15(9)12/h1-8H

27973-29-1 Relevant articles

Synthesis and electro-optical properties of carbazole-substituted pyrene derivatives

Jeong, Seonju,Park, Sung Hwan,Kim, Ki-Soo,Kwon, Younghwan,Ha, Ki-Ryong,Choi, Byeong-Dae,Han, Yoon Soo

, p. 4351 - 4356 (2011)

Mono and dicarbazole-substituted pyrene ...

A neutral state yellow to navy polymer electrochrome with pyrene scaffold

I?i-?zkut, Merve,?zta?, Zahide,Algi, Fatih,Cihaner, Atilla

, p. 1505 - 1511 (2011)

A new pyrene based soluble polymer, name...

Electrophilic Substitution of Monosubstituted Pyrenes

Minabe, Masahiro,Takeshige, Shouji,Soeda, Yuuji,Kimura,Takao,Tsubota, Motohiro

, p. 172 - 179 (1994)

Bromination and Friedel-Crafts acetylati...

Pyrene derivatives with two types of substituents at positions 1, 3, 6, and 8-fad or necessity?

Zych, Dawid,Slodek, Aneta

, p. 24015 - 24024 (2019)

1,3,6,8-Tetrasubstituted pyrene derivati...

A series of short axially symmetrically 1,3,6,8-tetrasubstituted pyrene-based green and blue emitters with 4-tert-butylphenyl and arylamine attachments

Zhang, Ran,Zhao, Yun,Zhang, Tengfei,Xu, Lu,Ni, Zhonghai

, p. 106 - 115 (2016)

A series of short axially symmetrically ...

1,8-Substituted Pyrene Derivatives for High-Performance Organic Field-Effect Transistors

Gong, Xiaojie,Zheng, Chaoyue,Feng, Xingcui,Huan, Yihong,Li, Jiewei,Yi, Mingdong,Fu, Zhenqian,Huang, Wei,Gao, Deqing

, p. 3920 - 3927 (2018)

There have been many reports on the appl...

Novel phenylcarbazole type organic compounds and an organic electroluminescent device comprising the same

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Paragraph 0157-0160, (2021/06/09)

An organic compound represented by chemi...

Electrochromic properties of pyrene conductive polymers modified by chemical polymerization

Chang, Lijing,Hou, Yanjun,Li, Rui,Ma, Yang,Miao, Shoulei,Wang, Cheng,Xu, Haoran,Zhang, Yuhang

, p. 39291 - 39305 (2021/12/27)

Pyrene is composed of four benzene rings...

Electron-Transfer-Induced Self-Assembly of a Molecular Tweezer Platform

Thakur, Khushabu,Wang, Denan,Mirzaei, Saber,Rathore, Rajendra

supporting information, p. 14085 - 14089 (2020/10/12)

The design and synthesis of a new molecu...

O-Doped Nanographenes: A Pyrano/Pyrylium Route Towards Semiconducting Cationic Mixed-Valence Complexes

Dor?evi?, Luka,Allain, Magali,Bonifazi, Davide,Coronado, Eugenio,Demitri, Nicola,Folli, Andrea,Mézière, Cécile,Ma?as-Valero, Samuel,Murphy, Damien,Sallé, Marc,Valentini, Cataldo

supporting information, p. 4106 - 4114 (2020/02/05)

Herein we report an efficient synthesis ...

27973-29-1 Process route

pyrene
129-00-0

pyrene

1,6-dibromopyrene
27973-29-1

1,6-dibromopyrene

Conditions
Conditions Yield
With bromine; In dichloromethane; at 20 ℃; for 30h;
64%
With bromine; In tetrachloromethane; at 110 ℃; for 12h; Darkness;
63%
With bromine; In chloroform; at 23 ℃; for 8h;
63%
With bromine; In tetrachloromethane; at 20 ℃; for 17h;
61%
With bromine; In dichloromethane; at 20 ℃; for 2h;
50%
With bromine; In dichloromethane; for 6h;
40%
With bromine; In tetrachloromethane; for 48h;
38.4%
With bromine; In chloroform; for 5h;
33%
With bromine; In chloroform; for 12h;
20%
With bromine; In chloroform;
17%
With bromine; In dichloromethane; at 20 ℃; for 24h; Inert atmosphere;
15%
With bromine; In chloroform; for 5h;
14.07%
With bromine; sodium bromide; In acetic acid;
With bromine; In tetrachloromethane;
With bromine; In tetrachloromethane; at 20 ℃;
7.6 g
With bromine; In dichloromethane;
With bromine; In dichloromethane;
With bromine; In tetrachloromethane; at 20 ℃;
With bromine; In tetrachloromethane;
pyrene
129-00-0

pyrene

1,6-dibromopyrene
27973-29-1

1,6-dibromopyrene

1,8-dibromopyrene
38303-35-4

1,8-dibromopyrene

Conditions
Conditions Yield
With carbon disulfide; bromine; at 20 ℃; for 17h;
85%
15%
With carbon disulfide; bromine; at 20 ℃; for 17h;
85%
15%
With bromine; In chloroform; for 4h; Inert atmosphere; Reflux;
71.1%
20%
With bromine; In tetrachloromethane; at 20 - 25 ℃; for 54h;
50%
25%
With bromine; In chloroform; at 20 ℃; for 5h;
14%
6%
With tetrachloromethane; bromine;
With bromine; In chloroform;
With mono(N,N,N-trimethylbenzenaminium) tribromide; zinc(II) chloride; In methanol; dichloromethane; at 20 ℃;
With bromine; In dichloromethane;
With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; In dichloromethane; at 20 ℃; for 1h;
With bromine; In tetrachloromethane; at 20 ℃; for 2h; Inert atmosphere;
With bromine; In tetrachloromethane;
With hydrogen bromide; dihydrogen peroxide; In methanol; diethyl ether; Inert atmosphere;
With bromine; In dichloromethane;
With hydrogen bromide; dihydrogen peroxide; In methanol; diethyl ether; Overall yield = 87.4 %; Inert atmosphere;
With bromine; In tetrachloromethane; at 20 ℃;
With bromine; In tetrachloromethane; at 20 ℃;
With bromine; In tetrachloromethane;
With bromine; In dichloromethane; at 20 ℃;
With tetrachloromethane; bromine; at 20 ℃; for 17h;
With hydrogen bromide; dihydrogen peroxide; In methanol; diethyl ether; water; at 20 ℃; for 24h; Overall yield = 74 percent; Overall yield = 8 g; Inert atmosphere;

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