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prop-2-en-1-yl (6S)-9-[ (1R)-1-(benzyloxy)ethyl]-12-[(benzyloxy)methyl]-2,2-dimethyl-4,7,10-trioxo-6-(propan-2-yl)-3-oxa-5,8,11-triazatridecan-13-oate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

452956-86-4

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  • prop-2-en-1-yl (6S)-9-[ (1R)-1-(benzyloxy)ethyl]-12-[(benzyloxy)methyl]-2,2-dimethyl-4,7,10-trioxo-6-(propan-2-yl)-3-oxa-5,8,11-triazatridecan-13-oate

    Cas No: 452956-86-4

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  • prop-2-en-1-yl (6S)-9-[ (1R)-1-(benzyloxy)ethyl]-12-[(benzyloxy)methyl]-2,2-dimethyl-4,7,10-trioxo-6-(propan-2-yl)-3-oxa-5,8,11-triazatridecan-13-oate

    Cas No: 452956-86-4

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452956-86-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 452956-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,5,2,9,5 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 452956-86:
(8*4)+(7*5)+(6*2)+(5*9)+(4*5)+(3*6)+(2*8)+(1*6)=184
184 % 10 = 4
So 452956-86-4 is a valid CAS Registry Number.

452956-86-4Relevant articles and documents

Formal total synthesis of stevastelins B and B3

Singh Yadav, Jhillu,Sekhar Mandal, Satadru,Srihari, Pabbaraja

, p. 669 - 688 (2014)

The formal total synthesis of stevastelins B and B3 (2 and 4, resp.) have been accomplished employing a highly enantiomerically controlled Lewis acid catalyzed non-aldol approach to obtain the syn aldol product and temperature controlled hydroboration oxidation reaction to construct four consecutive stereogenic centers. The other key reactions include Sharpless asymmetric epoxidation, macrolactonization, and macrolactamization towards building the core skeleton 2 and 4. Copyright

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