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1,2-bis(octadecyloxy)-4,5-bis[(trimethylsilyl)ethynyl]benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1246397-92-1 Structure
  • Basic information

    1. Product Name: 1,2-bis(octadecyloxy)-4,5-bis[(trimethylsilyl)ethynyl]benzene
    2. Synonyms:
    3. CAS NO:1246397-92-1
    4. Molecular Formula:
    5. Molecular Weight: 807.488
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1246397-92-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1,2-bis(octadecyloxy)-4,5-bis[(trimethylsilyl)ethynyl]benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-bis(octadecyloxy)-4,5-bis[(trimethylsilyl)ethynyl]benzene(1246397-92-1)
    11. EPA Substance Registry System: 1,2-bis(octadecyloxy)-4,5-bis[(trimethylsilyl)ethynyl]benzene(1246397-92-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1246397-92-1(Hazardous Substances Data)

1246397-92-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1246397-92-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,6,3,9 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1246397-92:
(9*1)+(8*2)+(7*4)+(6*6)+(5*3)+(4*9)+(3*7)+(2*9)+(1*2)=181
181 % 10 = 1
So 1246397-92-1 is a valid CAS Registry Number.

1246397-92-1Downstream Products

1246397-92-1Relevant articles and documents

Self-assembled monolayers of alkoxy-substituted octadehydrodibenzo[12] annulenes on a graphite surface: Attempts at peri-benzopolyacene formation by on-surface polymerization

Tahara, Kazukuni,Inukai, Koji,Hara, Noritaka,Johnson II, Charles A.,Haley, Michael M.,Tobe, Yoshito

, p. 8319 - 8328 (2010)

Self-assembled monolayers of a series of tetraalkoxy-substituted octadehydrodibenzo[12]annulene (DBA) derivatives 1c-g possessing butadiyne linkages were studied at the 1, 2, 4-trichlorobenzene (TCB) or 1-phenyloctane/graphite interface by scanning tunneling microscopy (STM). The purpose of this research is not only to investigate the structural variation of two-dimensional (2D) monolayers, but also to assess a possibility for peri-benzopolyacene formation by two-dimensionally controlled polymerization on a surface. As a result, the formation of three structures, porous, linear, and lamella structures, were observed by changing the alkyl chain length and the solute concentration. The formation of multilayers of the lamella structure was often observed for all compounds. The selection of molecular networks is basically ascribed to intermolecular and molecule-substrate interactions per unit area and network density. The selective appearance of the linear structure of Id is attributed to favorable epitaxial registry matching between the substrate lattice and the overlayer lattice. Even though the closest inter-atomic distance between the diacetylenic units of the DBAs in the lamella structure (≈0.6nm) is slightly larger compared to the typical distances necessary for topochemical polymerization, the reactivity toward external stimuli (electronic-pulse irradiation from an STM tip and UV irradiation) was investigated. Unfortunately, no evidence for polymerization of the DBAs on the surface was observed. The present results indicate the necessity for further designing a suitable system for the on-surface construction of structurally novel conjugated polymers, which are otherwise difficult to prepare.

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