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2-allyl-6-methoxy-benzoic acid (1R,3S,4R)-1-[2-(4-methoxy-benzyloxy)-ethyl]-3-methoxymethoxy-4,7-dimethyl-oct-6-enyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

312962-23-5

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312962-23-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 312962-23-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,2,9,6 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 312962-23:
(8*3)+(7*1)+(6*2)+(5*9)+(4*6)+(3*2)+(2*2)+(1*3)=125
125 % 10 = 5
So 312962-23-5 is a valid CAS Registry Number.

312962-23-5Relevant academic research and scientific papers

Asymmetric synthesis of the fully functional macrolide core of salicylihalamide: remote control of olefin geometry during RCM.

Fuerstner,Thiel,Blanda

, p. 3731 - 3734 (2007/10/03)

A catalysis-based approach to the core region 24 of the antitumor agents salicylihalamides A and B is reported. Key steps are two asymmetric hydrogenations of beta-keto esters 13 and 16 catalyzed by [(R)-BINAP.RuCl(2)](2).NEt(3) and an RCM-based macrocyclization effected by the NHC-containing ruthenium carbene 21. The stereochemical outcome of the latter reaction is controlled by remote substituents on the phenolic OH group of the cyclization precursor 23.

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