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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.

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  • 118132-04-0 Structure
  • Basic information

    1. Product Name: 1 2-DIBROMO-4 5-BIS(OCTYLOXY)BENZENE 9&
    2. Synonyms: 1 2-DIBROMO-4 5-BIS(OCTYLOXY)BENZENE 9&
    3. CAS NO:118132-04-0
    4. Molecular Formula: C22H36Br2O2
    5. Molecular Weight: 492.332
    6. EINECS: N/A
    7. Product Categories: Plasticizers;Polymer Additives;Polymer Science
    8. Mol File: 118132-04-0.mol
  • Chemical Properties

    1. Melting Point: 40-43 °C(lit.)
    2. Boiling Point: 485.7±40.0 °C(Predicted)
    3. Flash Point: >230 °F
    4. Appearance: /
    5. Density: 1.228±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1 2-DIBROMO-4 5-BIS(OCTYLOXY)BENZENE 9&(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1 2-DIBROMO-4 5-BIS(OCTYLOXY)BENZENE 9&(118132-04-0)
    11. EPA Substance Registry System: 1 2-DIBROMO-4 5-BIS(OCTYLOXY)BENZENE 9&(118132-04-0)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: 22-24/25
    4. WGK Germany: 3
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 118132-04-0(Hazardous Substances Data)

118132-04-0 Usage

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.

118132-04-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-dibromo-4,5-dioctoxybenzene

1.2 Other means of identification

Product number -
Other names -

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:118132-04-0 SDS

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

Synthesis and optoelectronic property manipulation of conjugated polymer photovoltaic materials based on benzo[d]-dithieno[3,2-b;2′,3′-f]azepine

Wang, Jian,Yin, Pan,Wu, Yue,Liu, Gangjian,Cui, Chaohua,Shen, Ping

, p. 184 - 195 (2018)

To develop new conjugated polymers (CPs) based on heteroepines, a soluble azepine moiety of benzo [d]-dithieno [3,2-b; 2′,3′-f]azepine was copolymerized with different building blocks to obtain a series of CPs. A broad absorption range of 300–850 nm and t

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

Physicochemical characterization of octakis(alkyloxy)-substituted Zn(II)-phthalocyanines non-covalently incorporated into an organogel and their remarkable morphological effect on the nanoscale-fibers

Diaz Diaz, David,Torres, Tomas,Zentel, Rudolf,Davis, Riju,Brehmer, Martin

, p. 2369 - 2371 (2008/02/12)

A series of octakis(alkyloxy)-substituted Zn(II)-phthalocyanines were efficiently incorporated into an organogel made of (1R,2R)-trans-1,2- bis(dodecanoylamino)cyclohexane by means of multiple cooperative non-covalent interactions, and SEM revealed the fo

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.

Control of the Discotic to Isotropic Transition in Alkoxy-Substituted Silicondihydroxo-Phthalocyanines by Axial Substituents

Sauer, Thomas,Wegner, Gerhard

, p. 97 - 118 (2007/10/02)

The synthesis of a homologous series of octaalkoxy-substituted silicondihydroxo-phthalocyanines is described.The mesomorphic properties of these new materials were studied by DSC, optical microscopy and X-ray investigations.Compounds with n >/= 4 (n is the number of carbon atoms in a single alkoxy side chain) show a discotic mesophase transition.A transition to the isotropic state is only observed when n >/= 8.X-ray diffraction patterns of the mesophases confirm that all compounds form a hexagonal columnar mesophase of the type Dhd.

Evidence of an ordered columnar mesophase in peripherally octa-n-alkoxy-substituted phthalocyanines

Pol, J. F. van der,Neeleman, E.,Zwikker, J. W.,Nolte, R. J. M.,Drenth, W.

, p. 615 - 620 (2007/10/02)

Liquid crystalline phthalocyanines with eight n-alkoxy chains have been synthesized and their mesophase structures determined by X-ray diffraction.The mesophases appear to be of the Dho type.Reasons for the preference of ordered columns are dis

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