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259209-16-0

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259209-16-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 259209-16-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,2,0 and 9 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 259209-16:
(8*2)+(7*5)+(6*9)+(5*2)+(4*0)+(3*9)+(2*1)+(1*6)=150
150 % 10 = 0
So 259209-16-0 is a valid CAS Registry Number.

259209-16-0Downstream Products

259209-16-0Relevant academic research and scientific papers

Cyclopropene cycloadditions with annulated furans: Total synthesis of (+)- and (-)-frondosin B and (+)-frondosin A

Oblak, E.Zachary,Vanheyst, Michael D.,Li, Jin,Wiemer, Andrew J.,Wright, Dennis L.

supporting information, p. 4309 - 4315 (2014/04/03)

The asymmetric total syntheses of the natural products (+)- and (-)-frondosin B and (+)-frondosin A are reported based on a diastereoselective cycloaddition between tetrabromocyclopropene and an annulated furan to provide a highly functionalized common bu

Novel and efficient one-step parallel synthesis of dibenzopyranones via suzuki-miyaura cross coupling

Vishnumurthy, Kodumuru,Makriyannis, Alexandros

experimental part, p. 664 - 669 (2010/11/04)

Microwave-promoted novel and efficient one-step parallel synthesis of dibenzopyranones and heterocyclic analogues from bromo arylcarboxylates and o-hydroxyarylboronic acids via Suzuki-Miyaura cross coupling reaction is described. Spontaneous lactonization

Synthetic and computational studies on liphagal: A natural product inhibitor of PI-3K

Zhang, Yanzhong,Oblak, E. Zachary,Bolstad, Erin S.D.,Anderson, Amy C.,Jasinski, Jerry P.,Butcher, Ray J.,Wright, Dennis L.

experimental part, p. 6120 - 6122 (2010/12/24)

The natural product liphagal has been shown to function as a reasonably potent and selective inhibitor of the key signaling enzyme PI-3Kα. We have been interested in developing an analog class of PI-3K inhibitors based upon this unusual terpenoid natural product. Toward that end, we have evaluated the binding of the natural product to its target protein computationally and formulated a class of simplified analogs based on the structural analysis. Utilizing the cycloadduct derived from tetrabromocyclopropene and furan, we were able to generate a key, versatile scaffold upon which to pursue this analog design.

Bipyridine manganese complexes

-

, (2008/06/13)

Compounds and methods of preparing compounds represented by structural formula (I): wherein X represents any suitable counter-anion; R1and R2independently represent hydrogen, C1-6alkoxy or nitro; R3, R4/su

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