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(3aS,4R,5R,6S,6aS)-4-benzyloxy-6-benzyloxymethyl-2-dimethylamino-3a,5,6,6a-tetrahydro-4H-cyclopentimidazole-5-yl acetamido-3,4,6-tri-O-benzyl-2-deoxy-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

774516-14-2

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774516-14-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 774516-14-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,4,5,1 and 6 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 774516-14:
(8*7)+(7*7)+(6*4)+(5*5)+(4*1)+(3*6)+(2*1)+(1*4)=182
182 % 10 = 2
So 774516-14-2 is a valid CAS Registry Number.

774516-14-2Downstream Products

774516-14-2Relevant academic research and scientific papers

Synthesis of a novel azapseudodisaccharide related to allosamidin employing N,N'-diacetylchitobiose as a key starting material

Takahashi, Shunya,Terayama, Hiroyuki,Koshino, Hiroyuki,Kuzuhara, Hiroyoshi

, p. 14871 - 14884 (2007/10/03)

Design and synthesis of a potential chitinase inhibitor 4, related to allosamidin (2), is described. Radical cyclization mediated by tributyltin hydride was applied for the first time to chitobiose-derived oxime ethers 9a,b to give four stereoisomers of an aminocyclopentane derivative connected to an N-acetyl-D- glucosamine residue at C-1 position. The major isomer 10b was efficiently converted into a novel pseudodisaccharide 4 via a series of cyclic-guanidine formation reaction.

Design and synthesis of a potential endoglycosidase inhibitor: Chemical conversion of N,N′-diacetylchitobiose into novel pseudodisaccharide containing a fivemembered cyclic N,N-dimethylguanidine

Takahashi, Shunya,Terayama, Hiroyuki,Koshino, Hiroyuki,Kuzuhara, Hiroyoshi

, p. 97 - 98 (2007/10/03)

(3aS,4R,5R,6R,6aS)-2-Dimethylamino-3a,5,6,6a-tetrahydro-4-hydroxy-6- hydroxymethyl-4H-cyclopentimidazole-5-yl 2-Acetamido-2-deoxy-β-D-glucopyranoside hydrochloride was designed as a potential inhibitor against endoglycosidases like lysozyme and chitinase, and was synthesized from N,N′-diacetylchitobiose by a series of reactions including radical cyclization of oxime ethers and cyclic guanidine-formation.

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