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methyl 4-azido-2,3-di-O-benzyl-4,6-dideoxy-α-D-mannopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

121803-79-0

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121803-79-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121803-79-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,8,0 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 121803-79:
(8*1)+(7*2)+(6*1)+(5*8)+(4*0)+(3*3)+(2*7)+(1*9)=100
100 % 10 = 0
So 121803-79-0 is a valid CAS Registry Number.

121803-79-0Relevant academic research and scientific papers

Synthesis of spacer-equipped di-, tri-, and the tetrasaccharide fragments of the deacetylated O-PS1 of Citrobacter gillenii O9a,9b, and a related pentasaccharide

Saksena, Rina,Chernyak, Anatoli,Kovac, Pavol

, p. 1693 - 1706 (2008/12/21)

The title rhamnooligosaccharides [α-d-Rhap4NAc-(1→3)-α-d-Rhap4NAc-1-O-(CH2)5COOMe, α-d-Rhap4NAc-(1→3)-α-d-Rhap4NAc-(1→3)-α-d-Rhap4NAc-1-O-(CH2)5COOMe, α-d-Rhap4NAc-(1→2)-α-d-Rhap4NAc-(1→3)-α-d-Rhap4NAc-(1→3)-α-d

Synthesis of specifically deoxygenated analogues of the methyl α-glycoside of the intracatenary monosaccharide repeating unit of the O-polysaccharide of Vibrio cholerae O:1

Gotoh, Makoto,Kovac, Pavol

, p. 73 - 84 (2007/10/02)

Treatment of methyl α-D-perosaminide (1) with γ-butyrolactone gave the 2'-deoxy analogue of methyl 4,6-dideoxy-4-(3-deoxy-L-glycero-tetronamido)-α-D-mannopyranoside (13), the methyl α-glycoside of the intracatenary monosaccharide repeating unit of the O-p

Block synthesis of two pentasaccharide determinants of the Brucella M antigen using thioglycoside methodologies

Peters, Thomas,Bundle, David R.

, p. 497 - 502 (2007/10/02)

Two frame shifted pentasaccharides containing 4,6-dideoxy-4-formamido-D-mannose (4-deoxy-4-formamido-D-rhamnose) have been synthesized by application of a strategy utilizing S-ethyl disaccharide glycoside building blocks 16 and 25.The target molecules con

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