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4,5-bis(2-ethylhexylthio)phthalonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1579998-63-2

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1579998-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1579998-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,9,9,9 and 8 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1579998-63:
(9*1)+(8*5)+(7*7)+(6*9)+(5*9)+(4*9)+(3*8)+(2*6)+(1*3)=272
272 % 10 = 2
So 1579998-63-2 is a valid CAS Registry Number.

1579998-63-2Relevant academic research and scientific papers

A Spin-Active, Electrochromic, Solvent-Free Molecular Liquid Based on Double-Decker Lutetium Phthalocyanine Bearing Long Branched Alkyl Chains

Zielinska, Agnieszka,Takai, Atsuro,Sakurai, Hiroya,Saeki, Akinori,Leonowicz, Marcin,Nakanishi, Takashi

, p. 770 - 774 (2018)

Synthesis and characterization of a novel, multifunctional, solvent-free room-temperature liquid based on alkylated double-decker lutetium(III) phthalocyanine (Pc2Lu) are described. Lowering of the melting point and viscosity of intrinsically solid Pc2Lu compounds has been achieved through the attachment of flexible, bulky, and long branched-alkyl chains, that is, thio-2-octyldodecyl, to the periphery of the Pc2Lu unit. The embedded Pc2Lu unit maintains its inherent molecular functions, such as spin-active nature and electrochromic behavior in the liquid state. Comparison of the properties with a solid-like Pc2Lu derivative, functionalized with shorter alkyl chains, that is, thio-2-ethylhexyl, underlines the importance of the hampering effect on the π–π interactions of neighboring Pc2Lu molecules by bulkier and longer branched-alkyl chains. This study could possibly pave the way for novel multifunctional liquids whose spin-activities are associated with their rheological or optoelectronic properties.

Electron-donating behavior of few-layer graphene in covalent ensembles with electron-accepting phthalocyanines

Ragoussi, Maria-Eleni,Katsukis, Georgios,Roth, Alexandra,Malig, Jenny,De La Torre, Gema,Guldi, Dirk M.,Torres, Tomás

supporting information, p. 4593 - 4598 (2014/04/17)

We describe herein the first example of highly exfoliated graphene covalently linked to electron accepting phthalocyanines. The functionalization of the nanocarbon surface with alkylsulfonyl phthalocyanines was attained by means of a click chemistry protocol. The new ensemble was fully characterized (thermogravimetric analysis, atomic force microscopy, transmission electron microscopy and Raman, as well as ground-state absorption) and was studied in terms of electron donor-acceptor interactions in the ground and in the excited state. In particular, a series of steady-state and time-resolved spectroscopy experiments demonstrated photoinduced electron transfer from the graphene to the electron-accepting phthalocyanines. This is the first example of an electron donor-acceptor nanoconjugate, that is, few-layer graphene/phthalocyanine, pinpointing the uncommon electron donating character of graphene.

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