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ethyl 2-O-acetyl-3-O-benzyl-4,6-O-benzylidene-1-thio-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

162681-47-2

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162681-47-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162681-47-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,6,8 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 162681-47:
(8*1)+(7*6)+(6*2)+(5*6)+(4*8)+(3*1)+(2*4)+(1*7)=142
142 % 10 = 2
So 162681-47-2 is a valid CAS Registry Number.

162681-47-2Downstream Products

162681-47-2Relevant academic research and scientific papers

HEPARAN SULFATE SYNTHESIS

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Page/Page column 28; 55-56, (2010/11/03)

The invention provides an efficient modular chemical synthesis for heparan sulfate oligosaccharides based on orthogonal protection strategies. Modular disaccharide building blocks, themselves the product of a novel combinatorial synthesis, are combined in

Modular synthesis of heparan sulfate oligosaccharides for structure-activity relationship studies

Arungundram, Sailaja,Al-Mafraji, Kanar,Asong, Jinkeng,Leach III, Franklin E.,Amster, I. Jonathan,Venot, Andre,Turnbull, Jeremy E.,Boons, Geert-Jan

supporting information; experimental part, p. 17394 - 17405 (2010/03/23)

Although hundreds of heparan sulfate binding proteins have been identified and implicated in a myriad of physiological and pathological processes, very little information is known about the ligand requirements for binding and mediating biological activiti

Synthesis of Methyl (Ethyl 2-O-acyl-3,4-di-O-benzyl-1-thio-β-D-glucopyranosid)uronates and Evaluation of Their Use as Reactive β-Selective Glucuronic Acid Donors

Garegg, Per J.,Olsson, Lars,Oscarson, Stefan

, p. 2200 - 2204 (2007/10/02)

The synthesis of derivatives of methyl (ethyl 2-O-acyl-3,4-di-O-benzyl-1-thio-β-D-glucopyranosid)uronate with different ester groups (acetyl, benzoyl, pivaloyl, and anisoyl) at O-2 is described.The synthesis proceeds via a two-step oxidation (DMSO/DCC fol

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