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130539-43-4

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130539-43-4 Usage

General Description

Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside is a chemical compound that is used in the field of organic chemistry and medicinal chemistry. It is a derivative of beta-D-glucopyranoside and contains a thiol group, a thio-beta-D-glucopyranoside moiety, and a unique 2H-isoindol-2-yl ring structure. Ethyl 2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-1-thio-beta-D-glucopyranoside may have potential applications in drug discovery and development due to its unique structural features and potential biological activities. Further research and studies are needed to explore the potential uses and effects of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 130539-43-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,0,5,3 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 130539-43:
(8*1)+(7*3)+(6*0)+(5*5)+(4*3)+(3*9)+(2*4)+(1*3)=104
104 % 10 = 4
So 130539-43-4 is a valid CAS Registry Number.

130539-43-4Downstream Products

130539-43-4Relevant articles and documents

ANTIMICROBIAL VACCINE COMPOSITIONS

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Paragraph 0081; 0085, (2021/03/05)

This invention is directed to antimicrobial vaccine compounds and compositions comprising oligosaccharide β-(1→6)- glucosamine groups having from 3 to 12 glucosamine units linked through a linker group to tetanus toxoid wherein the toxoid is primarily in

METHODS FOR PROVIDING CONTINUOUS THERAPY AGAINST PNAG COMPRISING MICROBES

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Paragraph 0078; 0082, (2021/05/29)

Disclosed are antimicrobial vaccines comprising oligosaccharide β-(1→6)-glucosamine groups.

Synthesis of Azido-Glycans for Chemical Glycomodification of Proteins

Wawryszyn, Mirella,Sauter, Paul F.,Nieger, Martin,Koos, Martin R. M.,Koehler, Christine,Luy, Burkhard,Lemke, Edward A.,Br?se, Stefan

, p. 4296 - 4305 (2018/08/29)

Chemically produced, accurately linkable oligosaccharides are of importance for the synthesis of neo-glycoproteins. On the route to high-mannose type N-glycans, we present a convenient synthesis of several glycans bearing an azide moiety at the reducing end. An azido-glycan core structure as valuable precursor was modified into the protected N-glycan pentasaccharide core structure and the possibility of modular attachment of different antenna was demonstrated through synthesis of a pentamannose donor and glycosylation with the core structure. The azido function allows for chemical ligation with recombinantly modified proteins featuring noncanonical cyclooctyne amino acids, providing access to customized glycopatterns of glycoproteins, e.g., of antibodies that are of high interest for biopharmaceutical applications.

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