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27069-36-9

1,4-Bis<2-(1-methylpyridinium-4-yl)vinyl>benzene diiodide is a photoisomerizable organic dye belonging to the class of distyrylpyridinium compounds. It exhibits reversible photoisomerization properties and interacts with DNA, showing potential as a DNA-binding ligand. 1,4-bis<2-(1-methylpyridinium-4-yl)vinyl>benzene diiodide's spectral and electrochemical properties are influenced by its structure, and it can serve as a fluorescent probe in various environments, including nanostructured materials like silica sol-gel matrices. Its behavior in polar solvents and solid matrices suggests applications in sensing and optoelectronic materials.

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  • 27069-36-9 Structure

  • Basic information

    1. Product Name: 1,4-bis<2-(1-methylpyridinium-4-yl)vinyl>benzene diiodide
    2. Synonyms: 1,4-bis<2-(1-methylpyridinium-4-yl)vinyl>benzene diiodide
    3. CAS NO:27069-36-9
    4. Molecular Formula:
    5. Molecular Weight: 568.239
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 27069-36-9.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<2-(1-methylpyridinium-4-yl)vinyl>benzene diiodide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,4-bis<2-(1-methylpyridinium-4-yl)vinyl>benzene diiodide(27069-36-9)
    11. EPA Substance Registry System: 1,4-bis<2-(1-methylpyridinium-4-yl)vinyl>benzene diiodide(27069-36-9)

  • 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: 27069-36-9(Hazardous Substances Data)

27069-36-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27069-36-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,0,6 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 27069-36:
(7*2)+(6*7)+(5*0)+(4*6)+(3*9)+(2*3)+(1*6)=119
119 % 10 = 9
So 27069-36-9 is a valid CAS Registry Number.

27069-36-9Downstream Products

27069-36-9Relevant articles and documents

Photoisomerizable DNA ligands. Spectral and electrochemical properties and base-pair selectivity of binding of bis[2-(1-alkylpyridinium-4- yl)vinyl]benzene dyes

Juskowiak, Bernard,Ohba, Mitsuyoshi,Sato, Masao,Takenaka, Shigeori,Takagi, Makoto,Kondo, Hiroki

, p. 265 - 277 (1999)

A series of bis [2-(alkylpyridinium-4-yl)vinyl]benzene ligands has been prepared and characterized, and their interactions with DNA have been studied by a combination of spectroscopic, hydrodynamic, and biochemical methods. Although bis[2-(1-alkylpyridini

Investigation of tetherable distilbazolium compounds as fluorescent probes in nanostructured silica sol-gel materials

Petrov,Cichos,Wagner,Spange,Von Borczyskowski

, p. 898 - 907 (2008/02/03)

Distibazolium dyes are investigated by steady-state and time-resolved fluorescence techniques in a series of low- and high-viscosity polar solvents and in a silica sol-gel matrix. In all solvents and the sol-gel matrix, an interplay of photoinduced switch

Synthesis of new 5-substituted 1,2,4-triazole-3-thione derivatives

Foks, Henryk,Czarnocka-Janowicz, Anna,Rudnicka, Waleria,Trzeciak, Henryk

, p. 67 - 81 (2007/10/03)

In the present paper we describe the preparation of series of new derivatives of 1,2,4-triazole-3-thiol. As starting materials methyl 3-acyldithiocarbazates were used, which on reaction with amines gave the corresponding 4,5-disubstituted 1,2,4-triazole-3-thiol derivatives (3). Into the 4-position of the 1,2,4-triazole-3-thiol system a β-hydroxyetlhyl substituent was introduced (compounds 4). These compounds were alkylated with methyl iodide to from 6, with N-substituted amides of chloroacetic acid (products 7 and 8), and aminomethylated with formation of Mannich bases (10). Some of the thiols 4 were desulfurized to 9. The new compounds were tested for their circulatory activity, but found not pharmacologically active.

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