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3-Butenoic acid, 2-hydroxy-3-methyl-, phenylmethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

20077-59-2

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20077-59-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20077-59-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,0,7 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 20077-59:
(7*2)+(6*0)+(5*0)+(4*7)+(3*7)+(2*5)+(1*9)=82
82 % 10 = 2
So 20077-59-2 is a valid CAS Registry Number.

20077-59-2Relevant academic research and scientific papers

Probing cytochrome P450-mediated activation with a truncated azinomycin analogue

Vinader, Victoria,Sadiq, Maria,Sutherland, Mark,Huang, Mengying,Loadman, Paul M.,Elsalem, Lina,Shnyder, Steven D.,Cui, Hongjuan,Afarinkia, Kamyar,Searcey, Mark,Patterson, Laurence H.,Pors, Klaus

, p. 187 - 191 (2015/02/05)

A deactivated alkene precursor (IC50 = 81 μM) to the azinomycin epoxide natural product can be bioactivated by several cytochromes P450 (CYP) to generate antiproliferative metabolites with increased potency (IC50 = 1-30 μM) in CHOwt cells. CYP1A1 and 3A4 were shown to generate exclusively the unnatural and the natural-configured azinomycin epoxide diastereoisomer respectively, while CYP1B1 produced both epoxides in a 3:1 mixture. The antiproliferative activity is linked to DNA damage as demonstrated using the comet assay. This journal is

Synthesis of (-)-octalactin A by a strategic vanadium-catalyzed oxidative kinetic resolution

Radosevich, Alexander T.,Chan, Vincent S.,Shih, Hui-Wen,Toste, F. Dean

, p. 3755 - 3758 (2008/12/23)

(Chemical Equation Presented) Both products of the kinetic resolution were used in the resolution/recombination approach shown in the scheme for the enantioselective total synthesis of (-)-octalactin A. Bn=benzyl, TBS=tert-butyldimethylsilyl.

Efficient stereoselective synthesis of the epoxyacid fragment of the azinomycins

Coleman, Robert S.,Sarko, Christopher R.,Gittinger, Jens P.

, p. 5917 - 5920 (2007/10/03)

Three concise enantioselective synthetic routes to the C17-C21 epoxyacid segment of the azinomycins are presented and were based on a Sharpless asymmetric epoxidation/kinetic resolution of racemic allylic alcohol (±)-3 that occurred with reversal of the expected sense of enantioselection.

Convenient synthesis of the epoxy fragment of azinomycin B

Konda,Machida,Sasaki,Takeda,Takayanagi,Harigaya

, p. 285 - 288 (2007/10/02)

A new convenient route for asymmetric synthesis of the epoxy fragment of azinomycin B by Sharpless asymmetric epoxidation of secondary allylic alcohol is described.

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