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(3R,4R)-(+)-trans-1-benzyloxycarbonyl-3,4-dihydroxypiperidine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

266688-41-9

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266688-41-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 266688-41-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,6,6,8 and 8 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 266688-41:
(8*2)+(7*6)+(6*6)+(5*6)+(4*8)+(3*8)+(2*4)+(1*1)=189
189 % 10 = 9
So 266688-41-9 is a valid CAS Registry Number.

266688-41-9Relevant academic research and scientific papers

Glycosynthase-Mediated Assembly of Xylanase Substrates and Inhibitors

Goddard-Borger, Ethan D.,Fiege, Brigitte,Kwan, Emily M.,Withers, Stephen G.

experimental part, p. 1703 - 1711 (2012/06/29)

An exo-β-xylosidase mutant with glycosynthase activity was created to aid in the synthesis of xylanase substrates and inhibitors. Simple monosaccharides were easily elaborated into di-, tri- and tetrasaccharides by using this enzyme. Some products proved

Biocatalytic preparation of enantioenriched 3,4-dihydroxypiperidines and theoretical study of Candida antarctica lipase B enantioselectivity

Solares, Laura F.,Lavandera, Iván,Gotor-Fernández, Vicente,Brieva, Rosario,Gotor, Vicente

, p. 3284 - 3291 (2007/10/03)

Enzymatic acetylations of N-substituted cis- and trans-3,4- dihydroxypiperidine and hydrolysis of their diacetylated derivatives have been studied. High enantioselectivities are obtained with Pseudomonas cepacia lipase and Candida antarctica lipase B for

Enantioselective Trans Dihydroxylation of Nonactivated C-C Double Bonds of Aliphatic Heterocycles with Sphingomonas sp. HXN-200

Chang, Dongliang,Heringa, Maarten F.,Witholt, Bernard,Li, Zhi

, p. 8599 - 8606 (2007/10/03)

The bacterial strain Sphingomonas sp. HXN-200 was used to catalyze the trans dihydroxylation of N-substituted 1,2,5,6-tetrahydropyridines 1 and 3-pyrrolines 4 giving the corresponding 3,4-dihydroxypiperidines 3 and 3,4-dihydroxypyrrolidines 6, respectivel

Nanomolar versus millimolar inhibition by xylobiose-derived azasugars: Significant differences between two structurally distinct xylanases

Williams, Spencer J.,Hoos, Roland,Withers, Stephen G.

, p. 2223 - 2235 (2007/10/03)

The synthesis of xylobiose-derived nitrogen-containing inhibitors of xylanase is described starting with accessible precursors through efficient synthetic schemes. Four disaccharides were identified as powerful competitive inhibitors of the retaining fami

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