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1-N-(4-nitrobenzoyl)-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

18918-52-0

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18918-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 18918-52-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,8,9,1 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 18918-52:
(7*1)+(6*8)+(5*9)+(4*1)+(3*8)+(2*5)+(1*2)=140
140 % 10 = 0
So 18918-52-0 is a valid CAS Registry Number.

18918-52-0Downstream Products

18918-52-0Relevant academic research and scientific papers

Synthesis of glucopyranosyl amides using polymer-supported reagents

Root, Yuriko Y.,Bailor, Maximillian S.,Norris, Peter

, p. 2499 - 2506 (2004)

2,3,4,6-Tetra-O-acetyl-β-D-glucopyranosyl azide reacts efficiently with polymer-supported triphenylphosphine and various acid chlorides to yield glucopyranosyl amides with retention of the β-gluco stereochemistry.

Application of bis(diphenylphosphino)ethane (DPPE) in Staudinger-type N-glycopyranosyl amide synthesis

Temelkoff, David P.,Smith, Craig R.,Kibler, Daniel A.,McKee, Shawn,Duncan, Sara J.,Zeller, Matthias,Hunsen, Mo,Norris, Peter

, p. 1645 - 1656 (2007/10/03)

Bis(diphenylphosphino)ethane (DPPE) reacts with pyranosyl azides derived from d-glucose and d-glucuronic acid in the presence of acid chlorides to yield the corresponding glycosyl amides. Reaction rates are comparable to those with triphenylphosphine, how

An easy access to anomeric glycosyl amides and imines (Schiff bases) via transformation of glycopyranosyl trimethylphosphinimides

Kovács, László,Osz, Erzsébet,Domokos, Valéria,Holzer, Wolfgang,Gy?rgydeák, Zoltán

, p. 4609 - 4621 (2007/10/03)

The preparation and application of anomeric glycosyl phosphinimides in preparative synthesis were studied. Starting from the appropriate glycosyl azides and trialkyl or triaryl phosphines, the corresponding phosphinimides were obtained by modified Staudin

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