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phenyl 3-O-acetyl-2-azido-4-O-benzyl-2-deoxy-1-thio-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

173465-75-3

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173465-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 173465-75-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,4,6 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 173465-75:
(8*1)+(7*7)+(6*3)+(5*4)+(4*6)+(3*5)+(2*7)+(1*5)=153
153 % 10 = 3
So 173465-75-3 is a valid CAS Registry Number.

173465-75-3Upstream product

173465-75-3Relevant academic research and scientific papers

Conformationally armed 3,6-tethered glycosyl donors: Synthesis, conformation, reactivity, and selectivity

Heuckendorff, Mads,Pedersen, Christian Marcus,Bols, Mikael

, p. 7234 - 7248 (2013/08/23)

The reactivity and selectivity of 3,6-tethered glycosyl donors have been studied using acceptors with different steric and electronic characteristics. Eight (four anomeric pairs) 3,6-bridged-glycosyl donors were synthesized in high yields from their common parent sugars. The glycosylation properties were tested using at least three different acceptors and several promoter systems. Thiophenyl 2,4-di-O-benzyl-3,6-O-(di-tert-butylsilylene)-α-d- glucopyranoside gave α/β mixtures with standard NIS/TfOH mediated activation, whereas the corresponding fluoride was found to be highly β-selective, when using SnCl2/AgB(C6F 5)4 as the promoter system. Mannosyl donors were highly α-selective despite the altered conformation. Galactosylations using NIS/TfOH were generally α-selective, but more β-selective using the galactosyl fluoride and depending on the acceptor used. Thiophenyl 2-azido-2-deoxy-4-O-benzyl-3,6-O-(di-tert-butylsilylene)-α-d- glucopyranoside was found to be α-selective. The reactivity of the donors was investigated using competition experiments, and some but not all were found to be highly reactive. Generally it was found that the α-thioglycosides were significantly more reactive than the β; this difference in reactivity was not found for 3,6-anhydro-, armed-(benzylated), or the classic super armed (silylated) donors. A mechanism supporting the unusual observations has been suggested.

Synthesis and biological evaluation of Rhizobium sin-1 lipid A derivatives

Demchenko, Alexei V.,Wolfert, Margreet A.,Santhanam, Balaji,Moore, James N.,Boons, Geert-Jan

, p. 6103 - 6112 (2007/10/03)

A highly convergent strategy for the synthesis of several derivatives of the lipid A of Rhizobium sin-1 has been developed. The approach employed the advanced intermediate 3-O-acetyl-6-O-(3-O-acetyl-4,6-O-benzylidene-2-deoxy-2-phthalimido- β-D-glucopyrano

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