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Benzene, 1,3-bis[(6-bromohexyl)oxy]-, also known as 1,3-bis(6-bromohexyloxy)benzene, is a chemical compound with the formula C18H27Br2O2. It is a colorless to light yellow liquid with a molecular weight of 414.218 g/mol. Benzene, 1,3-bis[(6-bromohexyl)oxy]is known for its use as a building block in the synthesis of polymers and as an intermediate in the production of specialty chemicals.

194854-06-3

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194854-06-3 Usage

Uses

Used in Polymer Synthesis:
Benzene, 1,3-bis[(6-bromohexyl)oxy]is used as a building block for the synthesis of polymers, contributing to the development of various polymeric materials with specific properties tailored for different applications.
Used in Specialty Chemicals Production:
Benzene, 1,3-bis[(6-bromohexyl)oxy]serves as an intermediate in the production of specialty chemicals, playing a crucial role in the creation of unique chemical compounds for specific industries.
Safety Precautions:

Check Digit Verification of cas no

The CAS Registry Mumber 194854-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,8,5 and 4 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 194854-06:
(8*1)+(7*9)+(6*4)+(5*8)+(4*5)+(3*4)+(2*0)+(1*6)=173
173 % 10 = 3
So 194854-06-3 is a valid CAS Registry Number.

194854-06-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis(6-bromohexoxy)benzene

1.2 Other means of identification

Product number -
Other names 1,3-bis(6-bromohexyloxy)benzene

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:194854-06-3 SDS

194854-06-3Downstream Products

194854-06-3Relevant academic research and scientific papers

Syntheses, Structural Studies, and Copper Iodide Complexes of Macrocycles Derived from Williamson Ether Syntheses Involving 2,9-Bis(4-hydroxyphenyl)-1,10-phenanthroline, α,ω-Dibromides, and Resorcinol or 2,7-Dihydroxynaphthalene

Baranová, Zuzana,Amini, Hashem,Neupane, Madhav,Garrett, Sydney C.,Ehnbom, Andreas,Bhuvanesh, Nattamai,Reibenspies, Joseph H.,Gladysz, John A.

, p. 373 - 386 (2017)

1,3-Bis(6-bromohexyloxy)benzene, 2,7-bis(6-bromohexyloxy)naphthalene, 1,3-bis(4-bromomethylbenzyloxy)benzene, and 1,3-bis(3-bromomethylbenzyloxy)benzene were prepared via Williamson ether synthesis using resorcinol or 2,7-dihydroxynaphthalene and 1,6-dibr

Synthesis, structure and catalytic activity of macrocyclic NHC PD pincer complexes

Watarai, Noriaki,Kawasaki, Hiroyasu,Azumaya, Isao,Yamasaki, Ryu,Saito, Shinichi

experimental part, p. 531 - 548 (2009/12/07)

We synthesized a series of new N-heterocyclic carbene (NHC) macrocyclic Pd pincer complexes (17-22) by the reaction of Pd(OAc)2 or Pd2(dba)3 with the corresponding macrocycles, which were prepared by the coupling reaction of dibromides with bisimidazoles. The complex adopted twisted conformation, and the activation energy of the conformational interconversion of the macrocycle was determined by VT-NMR. We also examined the catalytic activity of these Pd complexes in Mizoroki-Heck and oxidative alkynyl-alkynyl homocoupling reactions.

Template synthesis of [2]rotaxanes with large ring components and tris(biphenyl)methyl group as the blocking group. The relationship between the ring size and the stability of the rotaxanes

Saito, Shinichi,Nakazono, Kazuko,Takahashi, Eiko

, p. 7477 - 7480 (2007/10/03)

We synthesized a series of macrocyclic phenanthrolines 3a-e and a tris(biphenyl)methyl derivative 4. [2]Rotaxanes with large ring components (10a,b) were synthesized by the template method, and the stability of the rotaxanes was examined. The study reveal

Syntheses, X-ray structures and conformational studies of tetraoxa[n.n]metacyclophanes

Ogawa, Takuji,Kishimoto, Tomoaki,Kobayashi, Keijiro,Ono, Noboru

, p. 529 - 538 (2007/10/03)

New types of macrocyclic ligands with tetraoxa[n.n]metacyclophane molecular skeletons have been synthesized. The structures of 14,28-dibromo-1,8,15,22-tetraoxa[8.8]metacyclophane 2a, 16,32-dibromo-1,10,17,26-tetraoxa[10.10]metacyclophane 2b, 14,28-dibromo

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