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<2R,3R,6R,8R,8(1R),9S>-<3,9-dimethyl-8-<<1-methyl-2-(4-methoxybenzyl)oxy>ethyl>-1,7-dioxaspiro<5.5>undecan-2-yl>methanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

160238-53-9

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160238-53-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 160238-53-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,0,2,3 and 8 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 160238-53:
(8*1)+(7*6)+(6*0)+(5*2)+(4*3)+(3*8)+(2*5)+(1*3)=109
109 % 10 = 9
So 160238-53-9 is a valid CAS Registry Number.

160238-53-9Relevant academic research and scientific papers

Total synthesis of (+)-tautomycin

Shimizu, Satoshi,Nakamura, Sei-Ichi,Nakada, Masahisa,Shibasaki, Masakatsu

, p. 13363 - 13408 (2007/10/03)

A convergent stereocontrolled total synthesis of (+)-tautomycin (1), a specific inhibitor of protein serine/threonine phosphatases, has been achieved through an esterification of the C1.-C7. fragment A'74 with the C1-C26 fragment B'76 by a modified Yamaguchi method and an aldol reaction of the C17-C26 fragment C 5 with the C1-C16 fragment D 6 using LDA as key steps. The fragments 5 and 6 have been constructed in a stereocontrolled manner, respectively.

Synthetic studies on tautomycin. Stereoselective construction of the C1-C26 region

Nakamura, Sei-Ichi,Shibasaki, Masakatsu

, p. 4145 - 4148 (2007/10/02)

A convergent, stereocontrolled synthesis of the C1-C26 portion of tautomycin has been achieved through the coupling of the fragments 3 and 4 by an aldol condensation.

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