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1,2-Benzenedicarbonitrile, 3,6-bis[[(4-methylphenyl)sulfonyl]oxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 2,3-dicyano-4-[(4-methylbenzenesulfonyl)oxy]phenyl 4-methylbenzene-1-sulfonate

    Cas No: 667938-12-7

  • USD $ 1.9-2.9 / Gram

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  • 667938-12-7 Structure
  • Basic information

    1. Product Name: 1,2-Benzenedicarbonitrile, 3,6-bis[[(4-methylphenyl)sulfonyl]oxy]-
    2. Synonyms:
    3. CAS NO:667938-12-7
    4. Molecular Formula: C22H16N2O6S2
    5. Molecular Weight: 468.511
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 667938-12-7.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-Benzenedicarbonitrile, 3,6-bis[[(4-methylphenyl)sulfonyl]oxy]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,2-Benzenedicarbonitrile, 3,6-bis[[(4-methylphenyl)sulfonyl]oxy]-(667938-12-7)
    11. EPA Substance Registry System: 1,2-Benzenedicarbonitrile, 3,6-bis[[(4-methylphenyl)sulfonyl]oxy]-(667938-12-7)
  • 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: 667938-12-7(Hazardous Substances Data)

667938-12-7 Usage

Explanation

The molecular formula represents the number of atoms of each element present in a molecule of the compound.

Explanation

This is an alternative name for the compound, which is used to describe its structure and composition.

Explanation

The compound exists in a solid state and has a white, crystalline appearance.

Explanation

The compound is used as a key component in the synthesis of various polymers and resins, which are essential materials in the manufacturing of plastics, adhesives, and coatings.

Explanation

The compound serves as a crosslinking agent, which helps to strengthen and stabilize thermoset resins, a type of plastic that becomes rigid and infusible after being heated.

Explanation

Due to its chemical properties, the compound can cause irritation upon contact with the skin and eyes, necessitating careful handling and appropriate safety measures during its use.

Physical state

White crystalline solid

Applications

Production of polymers and resins

Use as a crosslinking agent

Thermoset resins

Safety precautions

Potential skin and eye irritant

Check Digit Verification of cas no

The CAS Registry Mumber 667938-12-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,6,7,9,3 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 667938-12:
(8*6)+(7*6)+(6*7)+(5*9)+(4*3)+(3*8)+(2*1)+(1*2)=217
217 % 10 = 7
So 667938-12-7 is a valid CAS Registry Number.

667938-12-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [2,3-dicyano-4-(4-methylphenyl)sulfonyloxyphenyl] 4-methylbenzenesulfonate

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:667938-12-7 SDS

667938-12-7Relevant articles and documents

Interaction between nickel hydroxy phthalocyanine derivatives with p-chlorophenol: Linking electrochemistry experiments with theory

Khene, Samson,Lobb, Kevin,Nyokong, Tebello

, p. 706 - 716 (2010)

In this work the interaction between peripherally (β) substituted nickel tetrahydroxyphthalocyanines (β-NiPc(OH)4 and β-Ni(O)Pc(OH)4) with p-chlorophenol is theoretically rationalised by performing calculations at B3LYP/6-31G(d) level. Density functional theory (DFT) and molecular orbital theory are used to calculate the condensed Fukui function for phthalocyanine derivatives and p-chlorophenol, in order to determine the reactive sites involved when p-chlorophenol is oxidized, and to compare theoretically predicted reactivity to experimentally determined electrocatalytic activity. Electrocatalytic activities of adsorbed NiPc derivatives: ads-α-NiPc(OH)8-OPGE (OPGE = ordinary poly graphite electrode), ads-α-NiPc(OH)4-OPGE and ads-β-NiPc(OH)4-OPGE are compared with those of the polymerized counterparts: poly-α-Ni(O)Pc(OH)8-OPGE, poly-α-NiPc(OH) 4-OPGE and poly-β-NiPc(OH)4-OPGE, respectively.

Far-red-absorbing cationic phthalocyanine photosensitizers: Synthesis and evaluation of the photodynamic anticancer activity and the mode of cell death induction

Machacek, Miloslav,Cidlina, Antonin,Novakova, Veronika,Svec, Jan,Rudolf, Emil,Miletin, Miroslav,Ku?era, Radim,Simunek, Tomas,Zimcik, Petr

, p. 1736 - 1749 (2015)

Novel zinc, magnesium, and metal-free octasubstituted phthalocyanine photosensitizers bearing [(triethylammonio)ethyl]sulfanyl substituents in the peripheral or nonperipheral positions were synthesized and investigated for their photophysical properties (

Tuning Optical and Electron Donor Properties by Peripheral Thio–Aryl Substitution of Subphthalocyanine: A New Series of Donor–Acceptor Hybrids for Photoinduced Charge Separation

Chandra B,Lim, Gary N.,D'Souza, Francis

, p. 13301 - 13311 (2016)

Subphthalocyanine (SubPc), a unique ring-reduced member of the common phthalocyanines family, although known for its higher absorptivity, reveals narrow absorption with peak maxima around 570 nm thus limiting its utility in light-energy-harvesting applica

METHODS FOR INCREASING EFFICIENCY AND STABILITY OF ORGANIC PEROVSKITE MATERIALS

-

Paragraph 0063, (2021/01/29)

The present invention provides methods for increasing stability and efficiency of organic perovskite materials for use in various electronic devices. In particular, methods of the invention use a non-peripheral substituted phthalocyanine for passivating d

Breaching the wall: morphological control of efficacy of phthalocyanine-based photoantimicrobials

Galstyan, Anzhela,Dobrindt, Ulrich

, p. 4630 - 4637 (2018/07/31)

An efficient treatment of infections using antimicrobial photodynamic therapy (aPDT) anticipates that uptake of photosensitizer (PS) by bacterial cells is very fast and effective. In this work, the design, synthesis, characterization, and photodynamic activity of amphiphilic, water-soluble zinc(ii)phthalocyanine (Zn(ii)Pc) molecules bearing none, three or six thiophenyl moieties are described. We show that PSs that contain no or flexible substituents on non-peripheral positions can photoinactivate microbes at very low loading concentrations and low light doses. In contrast, a PS derivative that contains non-flexible substituents is rendered less effective, despite an increased generation of cytotoxic singlet oxygen, higher lipophilicity and a lower tendency to aggregate. Our unexpected finding emphasizes the role of the morphology of PSs in bacterial cell-molecule interactions and suggests another relevant and hitherto disregarded characteristic to improve PS design.

Dye-sensitized solar cell and photoelectric conversion element and a phthalocyanine pigment used phthalocyanine dye

-

Paragraph 0054; 0055, (2017/06/02)

PROBLEM TO BE SOLVED: To provide a novel dye broad in the absorption wavelength range in the near infrared region and good in the phtoelectric conversion efficiency, and a photoelectric conversion device and a dye-sensitized solar cell using the same.SOLU

Synthesis of unsymmetrical carboxyphthalocyanines by palladium-catalyzed hydroxycarbonylation of iodo-substituted precursors

Aguirre De Carcer Garcia, Inigo,Sevim, Altug Mert,De La Escosura, Andres,Torres, Tomas

, p. 2237 - 2240 (2013/04/23)

Phthalocyanines (Pcs) containing a carboxylic acid functionality directly bound to the macrocycle have been synthesized, in one step and in good yields, from iodo-substituted Pc precursors. This methodology represents a convenient alternative to the commo

INFRARED ABSORBING MATERIAL, METHOD FOR SYNTHESIZING SAME, COLORING COMPOSITION, INK, TONER, PRINTED MATERIAL, IMAGE RECORDING METHOD AND IMAGE INFORMATION DETECTING METHOD

-

Page/Page column 20, (2012/02/04)

[PROBLEMS] To provide an infrared absorbing material which is readable with an infrared ray, and an ink, a toner, a printed matter, an image recording method and an image information detecting method that use the infrared absorbing material. [MEANS FOR SO

Rationally designed phthalocyanines having their main absorption band beyond 1000 nm

Kobayashi, Nagao,Furuyama, Taniyuki,Satoh, Koh

supporting information; experimental part, p. 19642 - 19645 (2012/01/19)

Highly air-stable phthalocyanines (Pcs) having their main absorption band beyond 1000 nm have been synthesized using main-group elements as peripheral and central (core) substituents. The resultant [(PhS)8PcP(OMe) 2][PF6]

Synthesis and electrochemical characterisation of new tantalum (V) alkythio phthalocyanines

Chauke, Vongani,Nyokong, Tebello

experimental part, p. 3662 - 3669 (2011/02/16)

The synthesis and electrochemical characterisation of octa-pentylthio (4a) and octa-octylthio (4b) - phthalocyaninato tantalum (III) hydroxide are hereby reported. These TaPc complexes absorb in the near infrared region (~800 nm in dichloromethane). They

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