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2-Butanone, 4-[(4-methoxyphenyl)methoxy]-4-[(1R,2R)-2-methylcyclopropyl]-, (4S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

879873-85-5

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879873-85-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 879873-85-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,9,8,7 and 3 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 879873-85:
(8*8)+(7*7)+(6*9)+(5*8)+(4*7)+(3*3)+(2*8)+(1*5)=265
265 % 10 = 5
So 879873-85-5 is a valid CAS Registry Number.

879873-85-5Relevant academic research and scientific papers

Enantioselective total synthesis of (-)-Clavosolide A and B

Son, Jung Beom,Kim, Si Nae,Kim, Na Yeong,Hwang, Min-Ho,Lee, Wonsun,Lee, Duck Hyung

scheme or table, p. 653 - 663 (2010/08/19)

Enantioselective total synthesis of (-)-clavosolide A and B was reported in full including the synthesis of proposed structure of (-)-clavosoldie A (1), revised structure of (-)-clavosoldie A (5), and revised structure of (-)-clavosoldie B (6). The relative and absolute stereochemistries of the natural products were confirmed unambiguously by comparing the optical rotation values and 1H and 13C NMR spectra of them.

Enantioselective total synthesis of (-)-clavosolide B

Son, Jung Beom,Hwang, Min-Ho,Lee, Wonsun,Lee, Duck-Hyung

, p. 3897 - 3900 (2008/02/11)

Enantioselective synthesis of 2, a revised structure for (-)-clavosolide B, was accomplished by a convergent approach, where syn-selective aldol, hydroxy-directed cyclopropanation, Mitsunobu inversion, Schmidt-type glycosylation, and macrolactonization re

Total synthesis, structural revision, and absolute configuration of (+)-clavosolide A

Son, Jung Beom,Kim, Si Nae,Kim, Na Yeong,Lee, Duck Hyung

, p. 661 - 664 (2007/10/03)

Enantioselective synthesis of 3, a revised structure for clavosolide A, was completed. Both 1H and 13C NMR spectra of the natural and synthetic compounds were identical, and optical rotation measurements identified the absolute confi

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