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(R)-5-((3-(methoxymethoxy)hexyl)thio)-1-phenyl-1H-tetrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

782498-34-4

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782498-34-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 782498-34-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,8,2,4,9 and 8 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 782498-34:
(8*7)+(7*8)+(6*2)+(5*4)+(4*9)+(3*8)+(2*3)+(1*4)=214
214 % 10 = 4
So 782498-34-4 is a valid CAS Registry Number.

782498-34-4Relevant academic research and scientific papers

Total synthesis of (+)-monocerin via tandem dihydroxylation-SN2 cyclization and a copper mediated tandem cyanation-lactonization approach

Nookaraju,Begari, Eeshwaraiah,Kumar, Pradeep

, p. 5973 - 5980 (2014/08/05)

A simple and novel synthesis of (+)-monocerin was achieved in 15 steps and 15.5% overall yield from 3-buten-1-ol employing hydrolytic kinetic resolution, Julia olefination, intramolecular tandem Sharpless asymmetric dihydroxylation-SN2 cyclizat

Facile entry to substituted decahydroquinoline alkaloids. Total synthesis of lepadins A-E and H

Pu, Xiaotao,Ma, Dawei

, p. 6562 - 6572 (2007/10/03)

Condensation of a L-alanine derived δ-bromo-β-silyloxy- propylamine with 1,3-cyclohexadione followed by alkylative cyclization produces a bicyclic enone. Diastereoselective Pt/C-catalyzed hydrogenation of this enone in HOAc provides a 5-oxo-cis-fused decahydroquinoline. Wittig olefination of this decahydroquinoline and subsequent epimerization of the resulting 5-formyl intermediate gives rise to a 5-β-formyl decahydroquinoline exclusively. In a parallel procedure, Peterson reaction of this decahydroquinoline and subsequent hydrogenation of the generated 5-exo-olefin provides a decahydroquinoline with a 5-α-substituent predominantly. For these two diastereoselective processes, using the intermediates without N-protection as the substrates is essential because the corresponding N-Boc intermediates give poor diastereoselectivity. The intermediate with β-form side chain is further converted into lepadins A-C via carbon chain elongation, while the intermediate with α-form side chain is transformed into lepadins D, E, and H and corresponding 5′-epimers via connection with two sulfones generated from two Sharpless epoxidation products. By comparison of the rotations and NMR data, the stereochemistry of lepadins D, E, and H is assigned as 2S,3R,4aS,5S,8aR,5′R.

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