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(R)-((4R,5S)-5-(tert-butyldiphenylsilyloxy)oct-7-en-4-yl) 2-(methoxymethoxy)hex-5-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1528757-97-2

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1528757-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1528757-97-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,2,8,7,5 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1528757-97:
(9*1)+(8*5)+(7*2)+(6*8)+(5*7)+(4*5)+(3*7)+(2*9)+(1*7)=212
212 % 10 = 2
So 1528757-97-2 is a valid CAS Registry Number.

1528757-97-2Downstream Products

1528757-97-2Relevant academic research and scientific papers

Stereoselective total synthesis of a novel regiomer of herbarumin i and its cytotoxic and antimicrobial activities

Jangili, Paramesh,Kashanna, Jajula,Kumar, C. Ganesh,Poornachandra,Das, Biswanath

, p. 325 - 327 (2015/02/19)

Stereoselective synthesis of a novel regiomer of the natural nonenolide, herbarumin I has been accomplished. The synthesis involves the coupling of the alcohol and acid fragments of the molecule using Yamaguchi protocol followed by intramolecular ring closing metathesis. The cytotoxic and antimicrobial properties of the synthetic regiomer have been studied.

Stereoselective total synthesis of a novel regiomer of herbarumin i and its cytotoxic and antimicrobial activities

Jangili, Paramesh,Kashanna, Jajula,Kumar, C. Ganesh,Poornachandra,Das, Biswanath

, p. 325 - 327 (2014/01/17)

Stereoselective synthesis of a novel regiomer of the natural nonenolide, herbarumin I has been accomplished. The synthesis involves the coupling of the alcohol and acid fragments of the molecule using Yamaguchi protocol followed by intramolecular ring closing metathesis. The cytotoxic and antimicrobial properties of the synthetic regiomer have been studied.

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