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1,3,2',6'-tetrakis(N-benzyloxycarbonyl)-5,6-O-cyclohexylideneneamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55728-75-1

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55728-75-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55728-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,7,2 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 55728-75:
(7*5)+(6*5)+(5*7)+(4*2)+(3*8)+(2*7)+(1*5)=151
151 % 10 = 1
So 55728-75-1 is a valid CAS Registry Number.

55728-75-1Downstream Products

55728-75-1Relevant articles and documents

Designed spiro-bicyclic analogues targeting the ribosomal decoding center

Cottin, Thomas,Pyrkotis, Constantina,Stathakis, Christos I.,Mavridis, Ioannis,Katsoulis, Ioannis A.,Anastasopoulou, Panoula,Kythreoti, Georgia,Zografos, Alexandros L.,Nahmias, Victoria R.,Papakyriakou, Athanasios,Vourloumis, Dionisios

experimental part, p. 71 - 87 (2011/12/16)

The bacterial ribosome represents the confirmed biological target for many known antibiotics that interfere with bacterial protein synthesis. Aminoglycosides represent a lead paradigm in RNA molecular recognition and constitute ideal starting points for t

Design of novel antibiotics that bind to the ribosomal acyltransfer site

Haddad, Jalal,Kotra, Lakshmi P.,Llano-Sotelo, Beatriz,Kim, Choonkeun,Azucena Jr., Eduardo F.,Liu, Meizheng,Vakulenko, Sergei B.,Chow, Christine S.,Mobashery, Shahriar

, p. 3229 - 3237 (2007/10/03)

The structure of neamine bound to the A site of the bacterial ribosomal RNA was used in the design of novel aminoglycosides. The design took into account stereo and electronic contributions to interactions between RNA and aminoglycosides, as well as a ran

TOTAL SYNTHESIS OF NEOMYCIN B

Usui, Takayuki,Umezawa, Sumio

, p. 133 - 144 (2007/10/02)

Total synthesis of neomycin B, a pseudo-tetrasaccharide aminoglycoside antibiotic, has been achieved through two key glycosylation reactions.Coupling of 3-O-acetyl-2,6-diazido-4-O-benzyl-2,6-dideoxy-L-idopyranosyl chloride with 5-O-benzoyl-1,2-O-isopropylidene-α-D-ribofuranose under modified Koenigs-Knorr conditions gave 70percent of the desired β-L disaccharide (3) and corresponding to neobiosamine in structure.After deisopropylidenation of 3 and acetylation, 1,2-di-O-acetyl-3-O-(3-O-acetyl-2,6-diazido-4-O-benzyl-2,6-dideoxy-β-L-idopyranosyl)-5-O-benzoyl-D-ribofuranose was coupled to HO-5 of 3,2',6'-tri-N-(benzyloxycarbonyl)-1-N:6-O-carbonyl-3',4'-di-O-(o-methoxybenzoyl)neamine, using trimethylsilyl trifluoromethanesulfonate, to give 60percent of the pseudo-tetrasaccharide 19 possessing the framework and masked functionality corresponding to neomycin B.Deblocking and reduction of the azido groups then gave neomycin B.

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