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3-azido-3-deoxy-6-O-toluene-p-sulphonyl-1,2-O-isopropylidene-α-D-glucofuranose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

22169-72-8

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22169-72-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22169-72-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,6 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22169-72:
(7*2)+(6*2)+(5*1)+(4*6)+(3*9)+(2*7)+(1*2)=98
98 % 10 = 8
So 22169-72-8 is a valid CAS Registry Number.

22169-72-8Relevant academic research and scientific papers

3,6-DIDEOXY-3,6-IMINO-1,2-O-ISODROPYLIDENE-α-D-GLUCOFURANOSE AS A DIVERGENT INTERMEDIATE FOR THE SYNTHESIS OF HYDROXYLATED PYRROLIDONES: SYNTHESIS IF 1,4-DIDEOXY-1,4-IMINO-L-GULITOL, 1,4-DIDEOXY-1,4-IMINO-D-LYXITOL, 2S,3S,4R,-3,4-DIHYDROXYPROLINE AND (1S,

Austin, Geoffrey N.,Baird, Peter D.,Fleet, George W. J.,Peach, Josephine M.,Smith, Paul W.,Watkin, David J.

, p. 3095 - 3108 (2007/10/02)

An efficient synthesis of the p-toluenesulphonate salt of 3,6-dideoxy-3,6-imino-1,2-O-isopropylidene-α-D-glucofuranose (1) from glucose is reported; the potential of (1) in making hydroxylated pyrrolidines is illustrated by the preparation of 1,4-dideoxy-

Synthesis of N-Acetyl Derivatives of (1R,5R)-6-Aza-2-oxabicyclooctan-3-one and (1S,5R,8R)-8-O-Benzyl-6-aza-2-oxabicyclooctan-3-one from D-Glucose

Gurjar, M. K.,Patil, V. J.,Pawar, S. M.

, p. 1115 - 1120 (2007/10/02)

N-Acetyl derivatives of (1R,5R)-6-aza-2-oxa-bicyclooctan-3-one (5) and (1S,5R,8R)-8-O-benzyl-6-aza-2-oxa-bicyclooctan-3-one (6), suitable chiral intermediates for (+)-retronecine (1) and (+)-crotanecine (2), have been synthesised from D-gluc

Digitoxigenin 3-O-β-D-Furanosides

Prisbe, Ernest J.,Verheyden, Julien P. H.,Montgomery, Wayne W.,Strosberg, Arthur M.

, p. 239 - 244 (2007/10/02)

The syntheses of the title compounds were accomplished by Koenig-Knorr condensation of acylated furanoses with digitoxigenin followed by basic hydrolysis of protecting groups.In this manner the riboside, 5-amino-5-deoxyriboside, 3,6-anhydroglucoside, and

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