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(S)-2-IodoMethyl-pyrrolidine-1-carboxylic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

172885-53-9

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172885-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 172885-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,8,8 and 5 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 172885-53:
(8*1)+(7*7)+(6*2)+(5*8)+(4*8)+(3*5)+(2*5)+(1*3)=169
169 % 10 = 9
So 172885-53-9 is a valid CAS Registry Number.

172885-53-9Relevant academic research and scientific papers

Copper-Catalyzed Reductive Trifluoromethylation of Alkyl Iodides with Togni's Reagent

Chen, Yanchi,Ma, Guobin,Gong, Hegui

supporting information, p. 4677 - 4680 (2018/08/07)

This work illustrates a reductive cross-electrophile coupling protocol for trifluoromethylation of alkyl iodides under Cu-catalyzed/Ni-promoted reaction conditions. The use of diboron esters as the terminal reductant allows the effective generation of the alkyl-CF3 products with excellent functional group tolerance and broad substrate scope. A mechanism involving a reaction of alkyl-Cu with Togni's reagent was proposed.

Synthesis of Nα-Z protected amino alkyl triazole acids and their application to neo-glycopeptides synthesis

Madhu, Chilakapati,Panguluri, Nageswara Rao,Sureshbabu, Vommina V.

, p. 858 - 864 (2014/08/05)

The synthesis of triazole linked glycopeptides employing 2-chloro-4,6-dimethoxy-1,3,5-triazine (CDMT) mediated coupling of Z-protected triazole acids with glycosyl amines and amino acid esters is described. The coupling proceeded smoothly at room temperat

Novel cyclic β-aminophosphonate derivatives as efficient organocatalysts for the asymmetric Michael addition reactions of ketones to nitrostyrenes

Widianti, Triana,Hiraga, Yoshikazu,Kojima, Satoshi,Abe, Manabu

experimental part, p. 1861 - 1868 (2010/11/18)

Three novel catalysts based upon cyclic β-aminophosphonate derivatives 13 were designed to catalyze the asymmetric Michael addition reactions of ketones to β-nitrostyrenes. Among the catalysts that have been prepared in this study, cyclic β-aminophosphonic acid monoethylester 3 showed the highest catalytic ability, giving the corresponding Michael adduct in good yields, high enantioselectivities (up to 92%ee), and high diastereoselectivities (syn:anti up to 95:5).

Catalytic antibodies in synthesis: Design and synthesis of a hapten for application to the preparation of a scalemic pyrrolidine ring synthon for ptilomycalin A

Anderson, Glen T.,Alexander, Michael D.,Taylor, Scott D.,Smithrud, David B.,Benkovic, Stephen J.,Weinreb, Steven M.

, p. 125 - 132 (2007/10/03)

A catalytic antibody-based approach toward the synthesis of an optically active pyrrolidine ring synthon potentially useful for ptilomycalin A is described. Enantiomerically pure hapten 37 was designed and constructed with the eventual goal of generating antibodies for the enantioselective partial hydrolysis of a mesoo diester such as 44 into a monoacid 45. This transition state analog possesses a phosphonate group containing the requisite oxyanionic character of the tetrahedral intermediate for ester hydrolysis. A newly developed carbamate-based linker, which was found to be much more hydrolytically stable than the commonly used glutarate ester, was developed for coupling of the hapten to a carrier protein.

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