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methyl N-t-butyloxycarbonyl-O-benzyl-2,6-dideoxy-2,6-imino-α-D-mannofuranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

105265-97-2

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105265-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 105265-97-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,2,6 and 5 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 105265-97:
(8*1)+(7*0)+(6*5)+(5*2)+(4*6)+(3*5)+(2*9)+(1*7)=112
112 % 10 = 2
So 105265-97-2 is a valid CAS Registry Number.

105265-97-2Relevant academic research and scientific papers

Methyl 2-azido-3-O-benzyl-2-deoxy-α-D-mamnofuranoside as a divergent intermediate for the synthesis of polyhydroxylated piperidines and pyrrolidines: synthesis of 2,5-dideoxy-2,5-imino-D-mannitol [2R,5R-dihydroxymethyl-3R,4R-dihydroxypyrrolidine]

Fleet, George W.J.,Smith, Paul W.

, p. 971 - 978 (2007/10/02)

The synthesis of methyl 2-azido-3-O-benzyl-2-deoxy-α-D-mannofuranoside (1) from D-glucose is reported; the conversions of (1) into derivatives of methyl 3-O-benzyl-2,6-dideoxy-2,6-imino-α-D-mannofuranoside (as precursors for the synthesis of polyhydroxylated piperidines) and into the hydroxylated pyrrrolidine, 2,5-dideoxy-2,5-imino-D-mannitol [2R,5R-dihydroxymethyl-3R,4R-dihydroxypyrrolidine] are described.

Synthesis of 2-Acetamido-1,5-imino-1,2,5-trideoxy-D-mannitol and of 2-Acetamido-1,5-imino-1,2,5-trideoxy-D-glucitol, a Potent and Specific Inhibitor of a Number of &β-N-Acetylglucosaminidases

Fleet, George W. J.,Smith, Paul W.,Nash, Robert J.,Fellows, Linda E.,Parekh, Raj B.,Rademacher, Thomas W.

, p. 1051 - 1054 (2007/10/02)

The stereochemical outcome of the azide displacement of triflates derived from a piperidin-3-ol depends on the protecting group on the ring nitrogen and allows the synthesis of 2-acetamido-1,5-imino-1,2,5-trideoxy-D-glucitol (a potent and specific inhibit

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