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methyl 2-azido-3-O-benzyl-2-deoxy-α-D-mannopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94119-09-2

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94119-09-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94119-09-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,1,1 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94119-09:
(7*9)+(6*4)+(5*1)+(4*1)+(3*9)+(2*0)+(1*9)=132
132 % 10 = 2
So 94119-09-2 is a valid CAS Registry Number.

94119-09-2Relevant articles and documents

Synthesis of a trisaccharide and a tetrasaccharide from the cell-wall lipopolysaccharides of Azospirillum brasilense S17

Pandey, Shashi,Ghosh, Samir,Misra, Anup Kumar

experimental part, p. 2584 - 2590 (2009/12/08)

A trisaccharide containing a D-mannosamine moiety and a tetrasaccharide containing an L-rhamnan chain that are found in the cell walls of Azospirillum brasilense S17 were synthesized concisely and in excellent yields. The key features of the synthetic str

Chemoenzymatic synthesis of CMP-N-acetyl-7-fluoro-7-deoxy-neuraminic acid

Hartlieb, Sina,Guenzel, Almut,Gerardy-Schahn, Rita,Muenster-Kuehnel, Anja K.,Kirschning, Andreas,Draeger, Gerald

, p. 2075 - 2082 (2008/12/21)

7-Fluoro sialic acid was prepared and activated as cytidine monophosphate (CMP) ester. The synthesis started with d-glucose, which was efficiently converted into N-acetyl-4-fluoro-4-deoxy-d-mannosamine. Aldolase catalyzed transformation yielded the corres

SYNTHESIS OF A TRISACCHARIDE COMPONENT OF THE CAPSULAR POLYSACCHARIDE OF Streptococcus pneumoniae TYPE 19F

Sugawara, Tamio,Igarashi, Kikuo

, p. 195 - 208 (2007/10/02)

2-O--α,β-L-rhamnopyranose, a structural component of the capsular polysaccharide of Streptococcus pneumoniae type 19F, has been synthesized by sequential glycosylation reactions using the gl

SYNTHESES OF 1,5-DIDEOXY-1,5-IMINO-D-MANNITOL FROM D-MANNOSE AND D-GLUCOSE

Fleet, G. W. J.,Gough, M. J.,Shing, T. K. M.

, p. 4029 - 4032 (2007/10/02)

Unambigous enantiospecific syntheses of 1,5-dideoxy-1,5-imino-D-mannitol (LU1, 1-deoxy-mannojirimycin) are reported (i) from D-mannose via hydrogenation of a 5-azido-5-deoxy mannose, and (ii) from D-glucose, in which the key step involves nucleophilic substitution of a trifluoromethanesulphonyl group from C-2 of D-glucose.

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