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(+)-[(2R,3S,6S)-2-(benzoyloxymethyl)-6-methoxyoxan-3-yl] benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

145593-73-3

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145593-73-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 145593-73-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,5,5,9 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 145593-73:
(8*1)+(7*4)+(6*5)+(5*5)+(4*9)+(3*3)+(2*7)+(1*3)=153
153 % 10 = 3
So 145593-73-3 is a valid CAS Registry Number.

145593-73-3Downstream Products

145593-73-3Relevant academic research and scientific papers

Diastereoselective synthesis of 2′,3′-dideoxy- β-C- glucopyranosides as intermediates for the synthesis of 2′,3′- dideoxy-β-D-glucopyranosyl-C-nucleosides

Loepfe, Michael,Siegel, Jay S.

, p. 1029 - 1035 (2008/09/17)

An extension of the Vorbrueggen method of nucleotide synthesis for the synthesis of C-glucopyranosides, as intermediates for C-nucleosides, is described. It could be shown that the diastereoselectivity of the reaction can be tuned by a simple change of protecting groups. Copyright Taylor & Francis Group, LLC.

Synthesis of hexopyranosyl acetates and 2,3-disubstituted tetrahydropyrans via chemoselective hydrogenation of hex-2-enopyranosyl acetates

Sasaki, Kaname,Wakamatsu, Takayuki,Matsumura, Shuichi,Toshima, Kazunobu

, p. 8271 - 8274 (2007/10/03)

A simple and easy method for chemoselective synthesis of hexopyranosyl acetates and 2,3-disubstituted tetrahydropyrans from hex-2-enopyranosyl acetates was demonstrated. The former was achieved by hydrogenation catalyzed by Rh/Al2O3

Synthesis and opioid-receptor binding of novel amino-substituted morphan analogues

Hoefner, Georg,Streicher, Benedikt,Wnsch, Bernhard

, p. 284 - 290 (2007/10/03)

Starting with methyl 4,6-O-benzylidene-α-D-glucopyranoside (4), an optimized procedure is reported for preparation of the bromide 7, which is transformed into the N-acylated heptopyranosamine 9. After introduction of an axially positioned azido moiety in

110. Warum Pentose- und nicht Hexose-Nucleinsaeuren? (Teil II) Oligonucleotide aus 2',3'-Dideoxy-β-D-glucopyranosyl-Bausteinen ('Homo-DNS'): Herstellung - Why Pentose and Not Hexose Nucleic Acids? Part II. Preparation of Oligonucleotides Containing 2',3'-

Boehringer, Markus,Roth, Hans-Joerg,Hunziker, Juerg,Goebel, Michael,Krishnan, Ravichandran,et al.

, p. 1416 - 1477 (2007/10/02)

This paper describes the preparation of the 2',3'-dideoxy-β-D-glucopyranosyl-(= 2',3'-dideoxy-β-D-erythro-hexapyranosyl)-derived nucleosides of the five bases adenine, cytosine, guanine, thymine, and uracil (= 'homo-deoxyribonucleosides') as well as the s

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