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606098-81-1

1,4-bis(hexyloxy)-2-(2-triisopropylsilylethynyl)-5-(2-trimethylsilylethynyl)benzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 606098-81-1 Structure

  • Basic information

    1. Product Name: 1,4-bis(hexyloxy)-2-(2-triisopropylsilylethynyl)-5-(2-trimethylsilylethynyl)benzene
    2. Synonyms: 1,4-bis(hexyloxy)-2-(2-triisopropylsilylethynyl)-5-(2-trimethylsilylethynyl)benzene
    3. CAS NO:606098-81-1
    4. Molecular Formula:
    5. Molecular Weight: 555.004
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 606098-81-1.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: 1,4-bis(hexyloxy)-2-(2-triisopropylsilylethynyl)-5-(2-trimethylsilylethynyl)benzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,4-bis(hexyloxy)-2-(2-triisopropylsilylethynyl)-5-(2-trimethylsilylethynyl)benzene(606098-81-1)
    11. EPA Substance Registry System: 1,4-bis(hexyloxy)-2-(2-triisopropylsilylethynyl)-5-(2-trimethylsilylethynyl)benzene(606098-81-1)

  • 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: 606098-81-1(Hazardous Substances Data)

606098-81-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 606098-81-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,6,0,9 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 606098-81:
(8*6)+(7*0)+(6*6)+(5*0)+(4*9)+(3*8)+(2*8)+(1*1)=161
161 % 10 = 1
So 606098-81-1 is a valid CAS Registry Number.

606098-81-1Relevant articles and documents

Experimental and Computational Studies of the Single-Molecule Conductance of Ru(II) and Pt(II) trans-Bis(acetylide) Complexes

Al-Owaedi, Oday A.,Milan, David C.,Oerthel, Marie-Christine,Bock, S?ren,Yufit, Dmitry S.,Howard, Judith A.K.,Higgins, Simon J.,Nichols, Richard J.,Lambert, Colin J.,Bryce, Martin R.,Low, Paul J.

, p. 2944 - 2954 (2016/11/03)

The single-molecule conductance of metal complexes of the general forms trans-Ru(C≡CArC≡CY)2(dppe)2 and trans-Pt(C≡CArC≡CY)2(PPh3)2 (Ar = 1,4-C6H2-2,5-(OC6H13/su

Self-assembled monolayers of clamped oligo(phenylene-ethynylene- butadiynylene)s

Jester, Stefan-S.,Schmitz, Daniela,Eberhagen, Friederike,Hoeger, Sigurd

, p. 8838 - 8840 (2011/09/14)

Rigid rod oligo(phenylene-ethynylene-butadiynylene)s (oPEBs), "half-rings" of two rigid rods connected via a molecular clamp unit, and shape-persistent macrocycles (cyclic "half-ring dimers") are synthesized and their self-assembled monolayers (SAMs) are

P-phenyleneethynylene molecular wires: Influence of structure on photoinduced electron-transfer properties

Wielopolski, Mateusz,Atienza, Carmen,Clark, Timothy,Guldi, Dirk M.,Martin, Nazario

supporting information; experimental part, p. 6379 - 6390 (2009/06/18)

A series of donor-acceptor arrays (exTTF-oPPE-C60) containing π-conjugated oligo(phenyleneethynylene) wires (oPPE) of different length between π-extended tetrathiafulvalene (exTTF) as electron donor and fullerene (C60) as electron acceptor has been prepared by following a convergent synthesis. The key reaction in these approaches is the bromo-iodo selectivity of the Hagihara-Sonogashira reaction and the deprotecting of acetylenes with different silyl groups to afford the corresponding donor-acceptor conjugates in moderate yields. The electronic interactions between the three electroactive species were determined by using UV-visible spectroscopy and cyclic voltammetry. Our studies clearly confirm that, although the C60 units are connected to the exTTF donor through π-conjugated oPPE frameworks, no significant electronic interactions are observed in the ground state. Theoretical calculations predict how a simple exchange from C=C double bonds (i.e., oligo(p-phenylenevinylene) to C≡C triple bonds (i.e., oPPE) in the electron donor-acceptor conjugates considerably alters long-range electron transfer. Photoexcitation of exTTF-oPPE-C 60 leads to the following features: a transient photoproduct with maxima at 660 and 1000 nm, which are unambiguously attributed to the photolytically generated radical-ion-pair state, [exTTF+-oPPE- C60-]. Both charge-separation and charge-recombination processes give rise to a molecular-wire behaviour of the oPPE moiety with an attenuation factor (β) of (0.2 ±0.05) A-1.

Rigid phenylene ethynylene units linked by a V-shaped centre. An approach to biaxial nematogens?

Lehmann, Matthias,Levin, Jeremy

, p. 273/[1315]-281/[1323] (2007/10/03)

Encouraged by theoretical predictions that nematic phases formed from V-shaped compounds could be biaxial, shape-persistent phenylene ethynylene arms linked by 1,3-phenylene, 4,4′-diphenylenemethane and 3,6-fluorenone units have been synthesized. Crystall

A giant conjugated molecular ring

Mayor, Marcel,Didschies, Claudia

, p. 3176 - 3179 (2007/10/03)

Ever increasing circles? The giant cycle 1 has a diameter of 12 nm making it the largest, shape persistent and monodisperse cyclic molecular structure designed and synthesized to date. A modular approach consisting of a series of subsequent dimerization s

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