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N-[(2S,3S,6S)-6-Allyloxy-2-(tert-butyl-dimethyl-silanyloxymethyl)-3,6-dihydro-2H-pyran-3-yl]-N-(2-bromo-allyl)-4-methyl-benzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

174467-57-3

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174467-57-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 174467-57-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,4,6 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 174467-57:
(8*1)+(7*7)+(6*4)+(5*4)+(4*6)+(3*7)+(2*5)+(1*7)=163
163 % 10 = 3
So 174467-57-3 is a valid CAS Registry Number.

174467-57-3Downstream Products

174467-57-3Relevant academic research and scientific papers

Palladium-mediated cyclisation on carbohydrate templates a new route to bis-annulated pyranosides

Nguefack, Jean-Flaubert,Bolitt, Veronique,Sinou, Denis

, p. 59 - 62 (1996)

A new and efficient route to bis-annulated pyranosides by palladium(0)-catalysed cascade cyclisation is described. The appropriate 2,3-unsaturated allylglycosides are subjected to Heck reaction under smooth Jeffery's conditions to produce the tricyclic de

Palladium-Mediated Cyclization on Carbohydrate Templates. 2. Synthesis of Enantiopure Tricyclic Compounds

Nguefack, Jean-Flaubert,Bolitt, Veronique,Sinou, Denis

, p. 6827 - 6832 (2007/10/03)

The bromo substituted unsaturated carbohydrates 3a-f were prepared from 3,4,6-tri-O-acetyl-D-glucal by Ferrier reaction with the appropriate allylic or homoallylic alcohol, deacetylation followed by monosilylation with TBDMSC1, and then alkylation with BrCH2CBr=CH2. The N- and C-analogues 4a,b were synthesized by palladium alkylation of the intermediate carbonate with TsNHCH2CBr=CH2 and (MeO2C)2,CHCH2CBr=CH2) respectively. Treatment of the unsaturated carbohydrates 3a, 4a, and 4b with a catalytic amount of Pd(OAc)2/PPh3 in CH3CN/H2O, in the presence of Bu4NHSO4 and NEt3, afforded the tricyclic compounds 5, 6, and 7, respectively. Under the same conditions, the analogue tricyclic compounds 8, 9, and 10 were formed starting from 3b-d. In the case of compounds 3e and 3f, the formation of the bicyclic glucal 11 via an already described β-alkoxyelimination was only observed. Moreover, trapping of the σ-alkylpalladium intermediate obtained from 3e with an external nucleophile yielded the 2-deoxy carbohydrate 12 and the 2,3-unsaturated sugar 13, using respectively sodium formate and sodium tetraphenylborate.

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