118132-04-0 Usage
Description
1,2-Dibromo-4,5-bis(octyloxy)benzene, also known as "9&", is a chemical compound with the molecular formula C22H36Br2O2. It is a symmetrical molecule with two bromine atoms and two octyloxy groups attached to a benzene ring. 1 2-DIBROMO-4 5-BIS(OCTYLOXY)BENZENE 9& is known for its symmetrical structure and chemical properties, making it a valuable component in the development of advanced materials for various technological applications.
Uses
Used in Organic Synthesis:
1,2-Dibromo-4,5-bis(octyloxy)benzene 9& is used as a building block for the synthesis of various organic compounds and materials. Its symmetrical structure and chemical properties make it a versatile component in the creation of new molecules with specific functions and applications.
Used in Electronics and Semiconductor Industries:
In the Electronics and Semiconductor Industries, 1,2-Dibromo-4,5-bis(octyloxy)benzene 9& is used as a precursor for manufacturing organic semiconductors and conducting polymers. Its unique chemical properties contribute to the development of advanced materials that are essential for the performance and efficiency of electronic devices and semiconductor components.
Used in Advanced Material Development:
1,2-Dibromo-4,5-bis(octyloxy)benzene 9& is also utilized in the development of advanced materials for a variety of technological applications. Its symmetrical structure and chemical properties allow for the creation of innovative materials with enhanced performance characteristics, such as improved conductivity, stability, and durability.
Check Digit Verification of cas no
The CAS Registry Mumber 118132-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,1,3 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 118132-04:
(8*1)+(7*1)+(6*8)+(5*1)+(4*3)+(3*2)+(2*0)+(1*4)=90
90 % 10 = 0
So 118132-04-0 is a valid CAS Registry Number.
118132-04-0Relevant articles and documents
Self-assembly of sulfur-containing heterocyclic compounds constructed by thianthrene units and their sulfonium salts
Hirabayashi, Kazunori,Ebine, Kenki,Kawabata, Youhei,Yoshida, Yoshihiro,Shimizu, Toshio
, (2018)
The self-assembly of sulfur-containing heterocyclic compounds, 5,6,11,12,17,18-hexathia-5,6,11,12,17,18-hexahydrotrinaphthylene and 5,7,12,14-tetrathiapentacene having octyloxy groups 1 and 2, was examined. Sulfides 1 and 2 self-assembled to form fibrous
Efficient synthesis of benzo fused tetrathia[7]helicenes
Waghray, Deepali,Nulens, Wienand,Dehaen, Wim
supporting information; experimental part, p. 5516 - 5519 (2011/12/22)
An efficient route toward the synthesis of symmetrical and unsymmetrical benzo fused tetrathia[7]helicenes substituted with electron donor (ED) and electron acceptor (EA) groups is reported. A common, readily available precursor 1,2- bis-(2-thienyl)benzen
SYNTHESIS AND CHARACTERIZATION OF SOLUBLE PHTHALOCYANINES: STRUCTURE-PROPERTY RELATIONSHIP
Hanack, Michael,Guel, Ahmet,Hirsch, Andreas,Mandal, Braja K.,Subramanian, L. R.,Witke, Elisabeth
, p. 365 - 382 (2007/10/02)
(μ-Oxo)bis 6a-c are obtained by treatment of the cyclotetramerisation product of 4,5-bis(alkoxy)-phthalonitriles in lithium pentanolate with iron(II) acetate.Compounds 6a-c are reduced to bisaxially coordinated octaalkoxyphthalocyaninatoiron(II) in the presence of ligands such as pyridine and t-butylisocyanide. reaction of 6a with bidentate bridging ligands (e.g. pyrazine, 1,4-dicyanobenzene) yields the bridged complexes 8a and 9a.The Moessbauer spectroscopic data are described and compared with the analogous unsubstituted phthalocyaninatoiron derivatives.