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(2R,3R,4S)-hex-5-yn-2,3,4-triol 2-benzoate ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

279684-68-3

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279684-68-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 279684-68-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,9,6,8 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 279684-68:
(8*2)+(7*7)+(6*9)+(5*6)+(4*8)+(3*4)+(2*6)+(1*8)=213
213 % 10 = 3
So 279684-68-3 is a valid CAS Registry Number.

279684-68-3Relevant academic research and scientific papers

Bronsted acid-promoted glycosylations of disaccharide glycal substructures of the saccharomicins

Balthaser, Bradley R.,McDonald, Frank E.

supporting information; experimental part, p. 4850 - 4853 (2009/12/28)

An acid-promoted glycosylate and alkynol cycloisomerization sequence provided direct access to the 2-deoxytrisaccharide corresponding to the fucose-saccharosamine-digitoxose substructure of saccharomicin B. In the course of this work, the absolute stereochemistry of the repeating fucose- saccharosamine disaccharide of saccharomicins was also confirmed.

Stereoselective glycosylations of a family of 6-deoxy-1,2-glycals generated by catalytic alkynol cycloisomerization

McDonald, Frank E.,Reddy, K. Subba,Diaz, Yolanda

, p. 4304 - 4309 (2007/10/03)

Photolysis of 0.25 equiv of W(CO)6 in the presence of tertiary amines (triethylamine or DABCO) and highly functionalized terminal alkynyl alcohols catalyzes single-step, high-yield cycloisomerization to endocyclic enol ethers. This transformati

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