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[(1S,2S,5S)-2-[3-(tert-butyldimethylsilanyloxy)propyl]-4-(tert-butyldiphenylsilanyloxymethyl)-2,5-dimethylcyclohex-3-enyl]-(10,10-dimethyl-3,3-dioxo-3λ6-thia-4-azatricyclo[5.2.1.01,5]dec-4-yl)-methanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

427897-76-5

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427897-76-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 427897-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,7,8,9 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 427897-76:
(8*4)+(7*2)+(6*7)+(5*8)+(4*9)+(3*7)+(2*7)+(1*6)=205
205 % 10 = 5
So 427897-76-5 is a valid CAS Registry Number.

427897-76-5Relevant academic research and scientific papers

Studies on the synthesis of the quartromicins: Partial stereochemical assignment of quartromicins A3 and D3 and diastereoselective synthesis of the endo- and exo-spirotetronate subunits

Roush, William R,Barda, David A,Limberakis, Chris,Kunz, Roxanne K

, p. 6433 - 6454 (2007/10/03)

A partial stereochemical assignment of quartromicins A3 and D3 is presented, along with diastereoselective syntheses of the endo- and exo-spirotetronates 1 and 2, corresponding to the galacto and agalacto fragments of the proposed quartromicin stereostructure. The key steps of these syntheses are highly enantio- and diastereoselective Lewis acid catalyzed Diels-Alder reactions of 1,1,3,4-tetrasubstituted diene 24.

Diastereoselective synthesis of the endo- and exo-spirotetronate subunits of the quartromicins. The first enantioselective Diels-Alder reaction of an acyclic (Z)-1,3-diene.

Roush, William R,Limberakis, Chris,Kunz, Roxanne K,Barda, David A

, p. 1543 - 1546 (2007/10/03)

[reaction: see text]. Diastereoselective syntheses of the endo- and exo-spirotetronates 1 and 2, corresponding to the galacto and agalacto fragments of quartromicins A3 and D3, are described. The key step of these syntheses are highly enantio- and diastereoselective Lewis acid catalyzed Diels-Alder reactions of the 1,1,3,4-tetrasubstituted diene 3.

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