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2-(4,4-dimethyl-2-oxazolin-2-yl)phenylthiol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

768370-65-6

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768370-65-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 768370-65-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,8,3,7 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 768370-65:
(8*7)+(7*6)+(6*8)+(5*3)+(4*7)+(3*0)+(2*6)+(1*5)=206
206 % 10 = 6
So 768370-65-6 is a valid CAS Registry Number.

768370-65-6Downstream Products

768370-65-6Relevant academic research and scientific papers

Dinuclear MoV Complexes with Thiophenolate-oxazoline Ligands: Synthesis, Characterization, and Exceptional Activity in Catalytic Olefin Epoxidation

Peschel, Lydia M.,Belaj, Ferdinand,Schachner, J?rg A.,M?sch-Zanetti, Nadia C.

, p. 2808 - 2817 (2017)

The synthesis, characterization, and epoxidation catalysis of two neutral, dinuclear molybdenum(V) complexes [{MoO(Lx)(μ-O)}2] (x = 1: 1; x = 2: 2) bearing S,N-bidentate thiophenolate-oxazoline ligands (L1, L2) are described. Both complexes are

Towards Structural-Functional Mimics of Acetylene Hydratase: Reversible Activation of Acetylene using a Biomimetic Tungsten Complex

Peschel, Lydia M.,Belaj, Ferdinand,M?sch-Zanetti, Nadia C.

, p. 13018 - 13021 (2015)

The synthesis and characterization of a biomimetic system that can reversibly bind acetylene (ethyne) is reported. The system has been designed to mimic catalytic intermediates of the tungstoenzyme acetylene hydratase. The thiophenyloxazoline ligand S-Pho

Glutathione peroxidase (GPx)-like antioxidant activity of the organoselenium drug ebselen: Unexpected complications with thiol exchange reactions

Sarma, Bani Kanta,Mugesh

, p. 11477 - 11485 (2005)

The factors that are responsible for the relatively low glutathione peroxidase (GPx)-like antioxidant activity of organoselenium compounds such as ebselen (1, 2-phenyl-1,2-benzisoselenazol-3(2H)-one) in the reduction of hydroperoxides with aromatic thiols

Activation and Photoinduced Release of Alkynes on a Biomimetic Tungsten Center: The Photochemical Behavior of the W?S-Phoz System

Peschel, Lydia M.,Vidovi?, Carina,Belaj, Ferdinand,Neshchadin, Dmytro,M?sch-Zanetti, Nadia C.

, p. 3893 - 3902 (2019/02/26)

The synthesis and structural determination of four tungsten alkyne complexes coordinated by the bio-inspired S,N-donor ligand 2-(4′,4′-dimethyloxazoline-2′-yl)thiophenolate (S-Phoz) is presented. A previously established protocol that involved the reaction of the respective alkyne with the bis-carbonyl precursor [W(CO)2(S-Phoz)2] was used for the complexes [W(CO)(C2R2)(S-Phoz)2] (R=H, 1 a; Me, 1 b; Ph, 1 c). Oxidation with pyridine-N-oxide gave the corresponding W-oxo species [WO(C2R2)(S-Phoz)2] (R=H, 2 a; Me, 2 b; Ph, 2 c). All W-oxo-alkyne complexes (2 a, b, c) were found to be capable of alkyne release upon light irradiation to afford five-coordinate [WO(S-Phoz)2] (3). The photoinduced release of the alkyne ligand was studied in detail by in situ 1H NMR measurements, which revealed correlation of the photodissociation rate constant (2 b>2 a>2 c) with the elongation of the alkyne C≡C bond in the molecular structures. Oxidation of [WO(S-Phoz)2] (3) with pyridine-N-oxide yielded [WO2(S-Phoz)2] (4), which shows highly fluxional behavior in solution. Variable-temperature 1H NMR spectroscopy revealed three isomeric forms with respect to the ligand arrangement versus each other. Furthermore, compound 4 rearranges to tetranuclear oxo compound [W4O4(μ-O)6(S-Phoz)4] (5) and dinuclear [{WO(μ-O)(S-Phoz)}2] (6) over time. The latter two were identified by single-crystal X-ray diffraction analyses.

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