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methyl 3-amino-4,6-O-benzylidene-2,3-dideoxy-3-C-methyl-α-D-ribo-hexopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98758-29-3

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98758-29-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98758-29-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,7,5 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 98758-29:
(7*9)+(6*8)+(5*7)+(4*5)+(3*8)+(2*2)+(1*9)=203
203 % 10 = 3
So 98758-29-3 is a valid CAS Registry Number.

98758-29-3Relevant academic research and scientific papers

Synthesis of D-rubranitrose by using a novel method for constructing functionalized branched-chain structures

Sato, Ken-Ichi,Miyama, Daisuke,Akai, Shoji

, p. 1523 - 1525 (2007/10/03)

Convenient synthesis of D-rubranitrose from D-glucose was achieved by using simple and novel methods for deoxygenation and construction of functionalized branched-chain structures. The total yield of D-rubranitrose from methyl 4,6-O-benzylidene-α-D-glucop

A New Stereoselective Route to Branched-Chain Nitro and Amino Sugars: Synthesis of Both Enantiomers of Decilonitrose and Avidinosamine

Greven, Ralph,Juetten, Peter,Scharf, Hans-Dieter

, p. 3742 - 3747 (2007/10/02)

Short, efficient, and highly diastereoselective syntheses of the title carbohydrates (15, 21, and 22), components of new anthracycline antibiotics, on a gram scale from readily available keto sugar precursors 6 and 17 are described.The syntheses feature t

Branched-chain Sugars. Part 18. Syntheses of D-Rubranitrose (2,3,6-Trideoxy-3-C-methyl-4-O-methyl-3-nitro-D-xylo-hexopyranose) and a Derivative of D-Kijanose (2,3,4,6-Tetradeoxy-4-methoxycarbonylamino-3-methyl-3-nitro-α-D-xylo-hexopyranose)

Brimacombe, John S.,Rahman, Khandker M. M.

, p. 1073 - 1080 (2007/10/02)

D-Rubranitrose (2,3,6-trideoxy-3-C-methyl-4-O-methyl-3-nitro-D-xylo-hexopyranose) (22), a constituent of the antibiotic rubradirin, has been synthesized from methyl 3,31-anhydro-4,6-O-benzylidene-2-deoxy-3-C-(hydroxymethyl)-α-D-arabino-hexopyr

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