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methyl 4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-3-(trifluoroacetamido)-α-D-ribo-hexopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

85687-32-7

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85687-32-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85687-32-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,8 and 7 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 85687-32:
(7*8)+(6*5)+(5*6)+(4*8)+(3*7)+(2*3)+(1*2)=177
177 % 10 = 7
So 85687-32-7 is a valid CAS Registry Number.

85687-32-7Downstream Products

85687-32-7Relevant academic research and scientific papers

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

SYNTHESIS AND ANTITUMOR ACTIVITY OF 3'-C-METHYL-DAUNORUBICIN

Thang, Ton That,Imbach, Jean Louis,Fizames, Christian,Lavelle, Francois,Ponsinet, Gerard,et al.

, p. 241 - 248 (2007/10/02)

Reaction of 1,5-anhydro-4-O-benzoyl-2,3,6-trideoxy-3-C-methyl-3-trifluoroacetamido-L-lyxo-hex-1-enitol with daunomycinone in the presence of anhydrous toluene-p-sulfonic acid in benzene, followed by removal of the N- and O-protecting groups under mild con

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