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(6R,7R,8S,8aR)-6,7-dihydroxy-8-benzyloxyhexahydrooxazolo[3,4-a]pyridin-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

791603-32-2

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791603-32-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 791603-32-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,1,6,0 and 3 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 791603-32:
(8*7)+(7*9)+(6*1)+(5*6)+(4*0)+(3*3)+(2*3)+(1*2)=172
172 % 10 = 2
So 791603-32-2 is a valid CAS Registry Number.

791603-32-2Relevant articles and documents

Stereoselective synthesis of 2-acetamido-1,2-dideoxynojirimycin (DNJNAc) and ureido-DNJNAc derivatives as new hexosaminidase inhibitors

De La Fuente, Alex,Mena-Barragán, Teresa,Farrar-Tobar, Ronald A.,Verdaguer, Xavier,García Fernández, José M.,Ortiz Mellet, Carmen,Riera, Antoni

, p. 6500 - 6510 (2015/06/16)

2-Acetamido-1,2-dideoxyiminosugars are selective and potent inhibitors of hexosaminidases and therefore show high therapeutic potential for the treatment of various diseases, including several lysosomal storage disorders. A stereoselective synthesis of 2-

General approach to glycosidase inhibitors. Enantioselective synthesis of deoxymannojirimycin and swainsonine

Martin, Ruben,Murruzzu, Caterina,Pericas, Miquel A.,Riera, Antoni

, p. 2325 - 2328 (2007/10/03)

(Chemical Equation Presented) Deoxymannojirimycin (2) and swainsonine (4) have been synthesized from each enantiomer of the same bicyclic carbarnate precursor 7. The key intermediate was prepared by a simple and efficient three-step synthesis involving RCM of the diene 8, which in turn is easily accessible in any configuration from enantiomerically enriched 2,3-epoxy-4-penten-1-ol 9.

Synthesis and biochemical properties of reversible inhibitors of UDP-N-acetylglucosamine 2-epimerase

Al-Rawi, Samy,Hinderlich, Stephan,Reutter, Werner,Giannis, Athanassios

, p. 4366 - 4370 (2007/10/03)

Sialic acids have important biochemical functions in healthy organisms, for example, in embryogenesis, as well as in the spread of diseases like influenza. A key step in the biosynthesis of the sialic acid N-acetylneuraminic acid is the epimerization of 1

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