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(1S,4R,5S,7S,8R)-8-Benzyloxy-7-methoxy-4-trifluoromethanesulfonyloxy-6-oxa-2-aza-bicyclo[3.2.1]octane-2-carboxylic acid benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

113000-80-9

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113000-80-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 113000-80-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,0,0 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 113000-80:
(8*1)+(7*1)+(6*3)+(5*0)+(4*0)+(3*0)+(2*8)+(1*0)=49
49 % 10 = 9
So 113000-80-9 is a valid CAS Registry Number.

113000-80-9Relevant academic research and scientific papers

SYNTHESIS OF DEOXYMANNOJIRIMYCIN FAGOMINE DEOXYNOJIRIMYCIN 2-ACETAMIDO-1,5-IMINO-1,2,5-TRIDEOXY-D-MANNITOL 2-ACETAMIDO-1,5-IMINO-1,2,5-TRIDEOXY-D-GLUCITOL 2S,3R,4R,5R-TRIHYDROXYPIPECOLIC ACID AND 2S,3R,4R,5S-TRIHYDROXYPIPECOLIC ACID FROM METHYL 3-O-BENZYL-2,6-DIDEOXY-2,6-IMINO-α-D-...

Fleet, George W. J.,Fellows, L. E.,Smith, Paul W.

, p. 979 - 990 (2007/10/02)

The value of methyl 3-O-benzyl-2,6-dideoxy-2,6-imino-α-D-mannofuranoside as a divergent intermediate for the preparation of polyhydroxylated piperidines is illustrated by the synthesis of deoxymannojirimycin (1,5-dideoxy-1,5-imino-D-mannitol), fagomine (1,5-imino-1,2,5-trideoxy-D-arabino-hexitol), deoxynojirimycin (1,5-dideoxy-1,5-imino-D-glucitol), 2-acetamido-1,5-imino-1,2,5-trideoxy-D-mannitol, 2-acetamido-1,5-imino-1,2,5-trideoxy-D-glucitol, 2S,3R,4R,5R-trihydroxypipecolic acid and 2S,3R,4R,5S-trihydroxypipecolic acid.

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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