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1-[2-(phenylthio)ethyl]piperidine is a chemical compound with the molecular formula C16H21NS. It is a derivative of piperidine, a cyclic amine, with a phenylthioethyl group attached to the nitrogen atom. 1-[2-(phenylthio)ethyl]piperidine is characterized by its unique structure, which features a six-membered piperidine ring and a phenylthioethyl side chain. The phenylthio group, which consists of a benzene ring attached to a sulfur atom, provides the compound with distinct chemical properties. 1-[2-(phenylthio)ethyl]piperidine is primarily used in the synthesis of various pharmaceuticals and agrochemicals due to its potential biological activity and reactivity. Its specific applications may vary depending on the desired end product, but its unique structure makes it a valuable building block in the development of new compounds with potential therapeutic or pesticidal properties.

1209-11-6

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1209-11-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1209-11-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1209-11:
(6*1)+(5*2)+(4*0)+(3*9)+(2*1)+(1*1)=46
46 % 10 = 6
So 1209-11-6 is a valid CAS Registry Number.

1209-11-6Relevant academic research and scientific papers

Aniline-Based Inhibitors of Influenza H1N1 Virus Acting on Hemagglutinin-Mediated Fusion

Leiva, Rosana,Barniol-Xicota, Marta,Codony, Sandra,Ginex, Tiziana,Vanderlinden, Evelien,Montes, Marta,Caffrey, Michael,Luque, F. Javier,Naesens, Lieve,Vázquez, Santiago

, p. 98 - 118 (2018/02/10)

Two series of easily accessible anilines were identified as inhibitors of influenza A virus subtype H1N1, and extensive chemical synthesis and analysis of the structure-activity relationship were performed. The compounds were shown to interfere with low pH-induced membrane fusion mediated by the H1 and H5 (group 1) hemagglutinin (HA) subtypes. A combination of virus resistance, HA interaction, and molecular dynamics simulation studies elucidated the binding site of these aniline-based influenza fusion inhibitors, which significantly overlaps with the pocket occupied by some H3 HA-specific inhibitors, indicating the high relevance of this cavity for drug design.

Synthesis and structural chemistry of N-{2-(arylthio/seleno)ethyl} morpholine/piperidine-palladium(II) complexes as potent catalysts for the Heck reaction

Singh, Pradhumn,Das, Dipanwita,Prakash, Om,Singh, Ajai K.

, p. 77 - 84 (2013/02/22)

The reactions of in-situ generated PhS-, PyS- and PhSe- with 4-(2-chloroethyl)morpholine hydrochloride and 1-(2-chloroethyl)piperidine hydrochloride in N2 atmosphere have resulted in N-{2-(arylchalcogeno)ethyl}morpholine/piperidine ligands (L1-L6), which on reaction with Na2PdCl4 at room temperature result in complexes of composition [PdCl2(L)] (1-6; L = L1-L6). All the complexes except 2 have been characterized by X-ray crystallography. The geometry around Pd is nearly square planar in all the cases. The Pd-S and Pd-Se bond lengths are in the ranges 2.2598(10)-2.2795(14) and 2.3541(6)-2.3632(15) ?, respectively. In 77Se{1H} NMR spectra of Pd(II)-complexes with L5 and L6 (Se ligands), the signals appear at higher frequency (up to 187 ppm) with respect to those of corresponding free ligands. Pd(II)-complexes (2, 4 and 6) have been found promising for Heck reaction of aryl bromides with methyl acrylate. The TON values are up to 18 200 and TOF up to 758 h-1 (with complex 6 as catalyst). The Pd-complexes of piperidene derivatives show little higher catalytic efficiency than those of morpholine ones. The positive Hg-test has implied that nano-sized Pd(0) species probably catalyze Heck reactions.

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