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Ethanamine, N-[(4-fluorophenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82605-86-5

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82605-86-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82605-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,6,0 and 5 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82605-86:
(7*8)+(6*2)+(5*6)+(4*0)+(3*5)+(2*8)+(1*6)=135
135 % 10 = 5
So 82605-86-5 is a valid CAS Registry Number.

82605-86-5Relevant academic research and scientific papers

Three novel Cd(II) dithiocarbamate complexes: synthesis, structural diversity and fluorescence properties

Singh, Ravi Pratap,Maurya, Vinay Kumar,Prasad, Lal Bahadur,Siddiqui, Kafeel Ahmad

, p. 2867 - 2876 (2020/07/03)

Three new homoleptic cadmium (II) dithiocarbamate complexes having molecular formula [Cd(KL)2], (KL1 = C15H13N1F1S2) (1); (L2 = C13H11N1F1S2) (2); (L3 = C11H14N1O1S2) (3), have been synthesized and characterized by elemental analysis, spectroscopy (IR, 1H and 13CNMR and UV–Vis). Single crystal X-ray studies confirm that the complex 1 crystallises in Orthorhombic with space group Pna21 and holding dimeric structure. In this complex Cd2+ having distorted octahedral geometry about the metal centre forms 1D coordination polymeric structures. The dimeric form of complex 2 and 3 crystallizes in triclinic crystal lattice with space group P-1.

Well-Defined Silica Grafted Molybdenum Bis(imido) Catalysts for Imine Metathesis Reactions

Barman, Samir,Merle, Nicolas,Minenkov, Yury,De Mallmann, Aimery,Samantaray, Manoja K.,Le Quéméner, Frédéric,Szeto, Kai C.,Abou-Hamad, Edy,Cavallo, Luigi,Taoufik, Mostafa,Basset, Jean-Marie

supporting information, p. 1550 - 1556 (2017/04/28)

Novel site-isolated tetracoordinated molybdenum complexes possessing bis(imido) ligands, [( - Si-O)2Mo( - NR)2] (R = t-Bu, 2,6-C6H3-i-Pr2), were immobilized on partially dehydroxylated silica (SiO2-200) by a rigorous surface organometallic chemistry protocol. The newly developed materials adorned with bis(imido) functional units, which were previously exploited mainly as spectator ligands on silica-supported olefin metathesis molybdenum catalysts, are found to be efficient heterogeneous catalytic systems for imine cross metathesis under mild conditions.

Palladium-catalyzed aryl iodide carbonylation as a route to imidazoline synthesis: Design of a five-component coupling reaction

Bontemps, Sebastien,Quesnel, Jeffrey S.,Worrall, Kraig,Arndtsen, Bruce A.

supporting information; body text, p. 8948 - 8951 (2011/10/19)

Take five: A new method employing aryl halide carbonylation to directly access heterocycles has been described (see scheme). In a single palladium-catalyzed reaction the catalyst mediates two consecutive carbonylation steps, thereby converting five components (aryl iodide, two units imine, and two units CO) into an imidazoline ring.

Dynamic asymmetric multicomponent resolution: Lipase-mediated amidation of a double dynamic covalent system

Vongvilai, Pornrapee,Ramstroem, Olof

supporting information; experimental part, p. 14419 - 14425 (2010/02/16)

The Strecker reaction is one of the most important multicomponent reactions developed, leading to R-aminonitriles that are versatile substrates for many synthetic applications. In the present study, this reaction type has been applied to a double dynamic covalent resolution protocol, leading to efficient C-C- and C-N-bond generation as well as chiral discrimination. The combination of transimination with iminecyanation enabled the dynamic exchange in more than one direction around a single stereogenic center of restricted structure. This multiple exchange process could generate a vast range of compounds from a low number of starting materials in very short time. The resulting double dynamic covalent systems, created under thermodynamic control, were subsequently coupled in a one-pot process with kinetically controlled lipase-mediated transacylation. This resulted in complete resolution of the dynamic systems, yielding the optimal N-acyl-α-aminonitriles for the enzyme, where the individual chemoenzymatic reactions could produce enantiomerically pure acylated N-substituted α-aminonitriles in good yields.

Reaction of Thiiranes with Azomethine Compounds

Sokolov, V. V.,Ogloblin, K. A.,Potekhin, A. A.

, p. 470 - 475 (2007/10/02)

Thiiranes add to imines and oximes to give thiazolidines.The addition of asymmetrical thiiranes is regioselective.The reaction of derivatives of asymmetrical carbonyl compounds with methylthiirane leads to mixtures of cis and trans stereoisomers of thiazo

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