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allyl (4-hydroxy)phenylacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

208932-52-9

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208932-52-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 208932-52-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,8,9,3 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 208932-52:
(8*2)+(7*0)+(6*8)+(5*9)+(4*3)+(3*2)+(2*5)+(1*2)=139
139 % 10 = 9
So 208932-52-9 is a valid CAS Registry Number.

208932-52-9Relevant academic research and scientific papers

Solid-phase synthesis of oligoesters using a JandaJel resin

Brümmer, Oliver,Clapham, Bruce,Janda, Kim D.

, p. 2257 - 2259 (2001)

This communication describes a general method for the solid-phase synthesis of oligomeric esters. A JandaJel resin was utilized as the solid support in conjunction with the highly acid labile Rink linker. Ester coupling reactions were performed using buff

Cysteine-based mannoside glycoclusters: Synthetic routes and antiadhesive properties

Schierholt, Alexander,Hartmann, Mirja,Schwekendiek, Kirsten,Lindhorst, Thisbe K.

scheme or table, p. 3120 - 3128 (2010/08/19)

Clustermannosides of different valency were synthesised based on cysteine. By employing the orthogonally protected amino acid as scaffold molecule, a variety of structurally varied products can be obtained according to different synthetic routes. Testing of the prepared glycoclusters as inhibitors of type 1 fimbriae mediated bacterial adhesion is reported, giving hints about the influence of sugar valency, sugar scaffolding, and the nature of the glycosidic aglycon in this testing system.

Design and synthesis of phosphotyrosine peptidomimetic prodrugs

Garrido-Hernandez, Hugo,Moon, Kyung D.,Geahlen, Robert L.,Borch, Richard F.

, p. 3368 - 3376 (2007/10/03)

A novel approach to the intracellular delivery of aryl phosphates has been developed that utilizes a phosphoramidate-based prodrug approach. The prodrugs contain an ester group that undergoes reductive activation intracellularly with concomitant expulsion

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