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1-acetyl-4,4-bis<3-bromo-4-(4-chlorobutoxy)-5-methylphenyl>piperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

108787-22-0

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108787-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108787-22-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,7,8 and 7 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 108787-22:
(8*1)+(7*0)+(6*8)+(5*7)+(4*8)+(3*7)+(2*2)+(1*2)=150
150 % 10 = 0
So 108787-22-0 is a valid CAS Registry Number.

108787-22-0Downstream Products

108787-22-0Relevant academic research and scientific papers

Designed Water-Soluble Macrocyclic Esterases: From Nonproductive to Productive Binding

Diederich, Francois,Schurmann, Gregor,Chao, Ito

, p. 2744 - 2757 (2007/10/02)

The synthesis and esterase properties of three water-soluble macrobicylic hosts, designed as α-chymotryspin mimics, are described.For supramolecular complexation in aqueous solution, host 1 possesses an apolar tetraoxaparacyclophane binding cavity, while hosts 2 and 4 have a larger tetraoxaparacyclophane binding site.A phenolic nucleophile is located atop the cavity of 1 and 2, while an alcoholic hydroxyl group is attached to 4.The multistep synthesis of hosts 1, 2, and 4 involves two macrocyclization reactions.A Williamson ether cyclization gives the tetraoxaparacyclophanes, and an amide cyclization attaches the nucleophiles to the binding sites.1H NMR host-guest complexation analysis demonstrates that both 1 and 2 form complexes of high stsbility with naphthalene guests in aqueous solution.In aqueous phosphate buffer at pH 8, host 2, with its partially ionized phenolic residue, is acylated much faster by complexed 4-nitro-1-naphthyl acetate (26) than host 4, which possesses the nonionized alcoholic hydroxyl group.The acylation of 2 by the complexed ester 26 is much faster than the hydrolysis of the ester in the presence of 1, a host with the same phenolic nucleophile but with a smaller binding site.The difference in esterase activity between 1 and 2 is explained in terms of productive versus nonproductive binding.The acylation of 2 by complexed ester 26 follows saturation kinetics whereas the hydrolysis of 26 in the presence of 1 obeys second-order kinetics.Host 2 shows a modest catalytic turnover in the hydrolysis of 26 in aqueous phosphate buffer at pH 8.The nature of catalysis provided by 2 is discussed.

PROGRESS TOWARDS ARTIFICIAL HYDROLASES: SYNTHESIS AND BINDING PROPERTIES OF A WATER-SOLUBLE CYCLOPHANE HOST WITH A PHENOL CAP

Schuermann, Gregor,Diederich, Francois

, p. 4249 - 4252 (2007/10/02)

The synthesis of the functionalized macrobicyclic host 1 on the way to the water-soluble artificial esterase 2 is presented.A phenolic nucleophile is properly oriented atop the binding cavity of 1 which forms strong complexes with aromatic guests in aqueo

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