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(-)-(1R)-(1α,2β,3β,4α,6β)-6-<(benzyloxycarbonyl)amino>-2-O,3-N-carbonyl-4-O-methyl-3-(methylamino)-1,2,4-cyclohexanetriol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121467-92-3

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121467-92-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121467-92-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,4,6 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 121467-92:
(8*1)+(7*2)+(6*1)+(5*4)+(4*6)+(3*7)+(2*9)+(1*2)=113
113 % 10 = 3
So 121467-92-3 is a valid CAS Registry Number.

121467-92-3Downstream Products

121467-92-3Relevant academic research and scientific papers

Aminoglycoside Antibiotics - Enantiomerically Pure Sannamine Building Blocks

Kuehlmeyer, Rainer,Seitz, Bernhard,Weller, Thomas,Fritz, Hans,Schwesinger, Reinhard,Prinzbach, Horst

, p. 1729 - 1744 (2007/10/02)

Starting from the prochiral dianhydrodeoxy-epi-inositol 9 a highly efficient synthesis for rac-sannamines (1, salts, derivatives) and rac-de-O-methylsannamine (18, salt) has been developed.Key steps are two regiospecific, practically quantitative epoxide opening reactions: intramolecularly in the diepoxyurethanes 11 and intermolecularly in the epoxyurethanes rac-13.With (R)-1-phenylethylamine as potential primary amino group in the second step separation of the corresponding diastereomers (16, 16') is achieved without significant loss of material.By this route enantiomerically pure (de-O-methyl)sannamines become available in which all functionalities are protected except that to be glycosidated.Attempts for an asymmetric realization of this synthesis resulted in only very small ee(de) values. - Key Words: Antibiotics, aminoglycoside/ Sannamine building blocks/ Aminoglycosides

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