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(S)-2-benzyloxycarbonylamino-4-methylpentyl thiolacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

744265-92-7

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744265-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 744265-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,4,2,6 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 744265-92:
(8*7)+(7*4)+(6*4)+(5*2)+(4*6)+(3*5)+(2*9)+(1*2)=177
177 % 10 = 7
So 744265-92-7 is a valid CAS Registry Number.

744265-92-7Relevant academic research and scientific papers

Novel sulfonamide-based carbamates as selective inhibitors of bche

?těpánková, ?árka,Enriz, Ricardo D.,Garro, Adriana D.,Ho?ek, Jan,Imramovsky, Ale?,Jampílek, Josef,Jendrzejewska, Izabela,Magar, Pratibha,Parravicini, Oscar,Pauk, Karel,Svr?ková, Katarina

, (2021/09/04)

A series of 14 target benzyl [2-(arylsulfamoyl)-1-substituted-ethyl]carbamates was prepared by multi-step synthesis and characterized. All the final compounds were tested for their abil-ity to inhibit acetylcholinesterase (AChE) and butyrylcholinesterase

SuFExable Isocyanides for Ugi Reaction: Synthesis of Sulfonyl Fluoro Peptides

Xu, Shuheng,Cui, Sunliang

supporting information, p. 5197 - 5202 (2021/07/20)

Herein, the sulfonyl fluoro isocyanides were first developed as a new type of SuFExable synthon, and they are used as building blocks in the Ugi reaction (U-4CR). The Ugi reaction was established and the substrate scope was investigated, and various sulfonyl fluoro α-amino amides and peptides could be reached in a one-step synthesis. Therefore, this protocol opens a new vision for SuFExable building blocks and click chemistry, and it also provides a distinct approach to sulfonyl fluoro peptides.

Selective inhibition of the immunoproteasome by ligand-induced crosslinking of the active site

Dubiella, Christian,Cui, Haissi,Gersch, Malte,Brouwer, Arwin J.,Sieber, Stephan A.,Krüger, Achim,Liskamp, Rob M. J.,Groll, Michael

supporting information, p. 11969 - 11973 (2015/03/04)

The concept of proteasome inhibition ranks among the latest achievements in the treatment of blood cancer and represents a promising strategy for modulating autoimmune diseases. In this study, we describe peptidic sulfonyl fluoride inhibitors that selecti

An efficient and facile synthesis of N-Cbz-β-aminoalkanesulfonamides

Meng, Fanhua,Chen, Ning,Xu, Jiaxi

, p. 2548 - 2553 (2013/06/27)

An efficient method for the synthesis of N-Cbz-β- aminoalkanesulfonamides was described. N-Cbz-β-aminoalkanesulfona-mides were readily prepared in good yields from a variety of amino alcohols, including optically active ones, via N-Cbz protection with ben

Synthesis and biological evaluation of novel irreversible serine protease inhibitors using amino acid based sulfonyl fluorides as an electrophilic trap

Brouwer, Arwin J.,Ceylan, Tarik,Jonker, Anika M.,Linden, Tima Van Der,Liskamp, Rob M.J.

scheme or table, p. 2397 - 2406 (2011/05/12)

We have designed and synthesized novel irreversible serine protease inhibitors containing aliphatic sulfonyl fluorides as an electrophilic trap. These substituted taurine sulfonyl fluorides derived from taurine or protected amino acids were conveniently s

Synthesis of β-aminoethanesulfonyl fluorides or 2-substituted taurine sulfonyl fluorides as potential protease inhibitors

Brouwer, Arwin J.,Ceylan, Tarik,Linden, Tima van der,Liskamp, Rob M.J.

scheme or table, p. 3391 - 3393 (2009/09/05)

Substituted taurine sulfonyl fluorides derived from taurine or protected amino acids are conveniently synthesized from β-aminoethanesulfonyl chlorides using KF/18-crown-6 or from β-aminoethanesulfonates using DAST.

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