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(Z)-(6S,7R,8S)-7-(tert-butyldimethylsilanyloxy)-9-(4-methoxybenzyloxy)-4,6,8-trimethylnon-4-enoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

373645-85-3

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373645-85-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 373645-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,7,3,6,4 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 373645-85:
(8*3)+(7*7)+(6*3)+(5*6)+(4*4)+(3*5)+(2*8)+(1*5)=173
173 % 10 = 3
So 373645-85-3 is a valid CAS Registry Number.

373645-85-3Downstream Products

373645-85-3Relevant academic research and scientific papers

Synthesis of (Z)-Trisubstituted olefins by decarboxylative Grob-Type fragmentations: Epothilone D, discodermolide, and peloruside A

Prantz, Kathrin,Mulzer, Johann

experimental part, p. 485 - 506 (2010/06/14)

Methyl-branched (Z)-trisubstituted olefins are found in many polyketides with interesting biological activity, such as epothilone D (1), discodermolide (3), and peloruside A (2). Despite the employment of numerous different strategies, this motif has often been the weak point in total synthesis. Thus, we present a novel hydroxideinduced Grob-type fragmentation as an easy access to trisubstituted olefins. In our case, β-mesyloxy δ-lactones with three stereogenic centers were chosen whose fragmentation underlies a high stereoelectronic control. Major challenges in the syntheses were the instailation of quaternary stereocenters, achieved by enzymatic desymmetrization of meso-diesters and by aluminiumpromoted stereoselective rearrangement of chiral epoxides, respectively. Different aldol strategies were developed for the formation of the fragmentation precursors. Additionally a short survey about nucleophilic additions to aldehydes with quaternary α-centers is presented.

A practical synthesis of (+)-discodermolide and analogues: Fragment union by complex aldol reactions

Paterson,Florence,Gerlach,Scott,Sereinig

, p. 9535 - 9544 (2007/10/03)

A practical stereocontrolled synthesis of (+)-discodermolide (1) has been completed in 10.3% overall yield (23 steps longest linear sequence). The absolute stereochemistry of the C1-C6 (7), C9-C16 (8), and Csub

Total synthesis of the antimicrotubule agent (+)-discodermolide using boron-mediated aldol reactions of chiral ketones

Paterson, Ian,Florence, Gordon J.,Gerlach, Kai,Scott, Jeremy P.

, p. 377 - 380 (2007/10/03)

With a similar mechanism of action to taxol, the title compound 1 is a particularly promising candidate for development in cancer chemotherapy. This efficient synthesis, based on stereocontrolled aldol reactions, should help to overcome the scarce natural

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