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(3E)-7-(N-tert-butoxycarbonyl)amino-2,3,7-trideoxy-4,5-O-isopropylidene-1-C-phenyl-D-xylo-hept-2-en-1-ulose is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

196406-73-2

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196406-73-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 196406-73-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,6,4,0 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 196406-73:
(8*1)+(7*9)+(6*6)+(5*4)+(4*0)+(3*6)+(2*7)+(1*3)=162
162 % 10 = 2
So 196406-73-2 is a valid CAS Registry Number.

196406-73-2Relevant academic research and scientific papers

The synthesis of ester and ketone analogues of 1-deoxynojirimycin and castanospermine

Compernolle, Frans,Joly, Gert,Peeters, Koen,Toppet, Suzanne,Hoornaert, Georges,Kilonda, Amuri,Babady-Bila

, p. 12739 - 12754 (1997)

1-Amino-1-deoxy-D-glucitol (3) was converted into the 3,4;5,6-di-O-isopropylidene protected ammonium salt 17 which was transformed further into the trans-fused piperidine acetonides 4-8 in six steps and 23-32% overall yield. In the final step, ring closur

The Synthesis of 7-Carbonyl Homologues of 1-Deoxynojirimycin

Kilonda, Amuri,Compernolle, Frans,Toppet, Suzanne,Hoornaert, Georges J.

, p. 9047 - 9050 (2007/10/02)

A 3,4;5,6-di-O-isopropylidene salt derivative of 1-amino-1-deoxy-D-glucitol was transformed to N-Boc protected (5,6)-α,β-unsaturated 7-carbonyl compounds.Conversion to the title piperidine products proceeded via deprotection and intramolecular 1,4-additio

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