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methyl 2-(5-methoxy-2-nitrophenyl)-2-methylpropanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

136764-91-5

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136764-91-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 136764-91-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,6,7,6 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 136764-91:
(8*1)+(7*3)+(6*6)+(5*7)+(4*6)+(3*4)+(2*9)+(1*1)=155
155 % 10 = 5
So 136764-91-5 is a valid CAS Registry Number.

136764-91-5Relevant academic research and scientific papers

Total Synthesis of 4,5-Didehydroguadiscine: A Potent Melanogenesis Inhibitor from the Brazilian Medicinal Herb, Hornschuchia obliqua

Tanabe, Genzoh,Sugano, Youta,Shirato, Miki,Sonoda, Naoki,Tsutsui, Nozomi,Morikawa, Toshio,Ninomiya, Kiyofumi,Yoshikawa, Masayuki,Muraoka, Osamu

, p. 1536 - 1542 (2015)

The first total synthesis of the 7,7-dimethylaporphinoid, 4,5-didehydroguadiscine (6), originally isolated from the stems and roots of Hornschuchia oblique (Annonaceae), was achieved by the condensation of homopiperonylamine (7) with an α,α-dimethylphenylacetic acid derivative (8) and subsequent Pschorr reaction of the resulting benzylisoquinoline intermediate (22). The reported 13C NMR data were partially revised on the basis of the analysis of HMBC spectra measured under different conditions. The melanogenesis inhibitory activity (IC50 = 4.7 μM) of 6 was 40 times stronger than that of arbutin (174 μM), which was used as reference standard. Furthermore, 6 was the most potent natural melanogenesis inhibitor within this class of compounds. (Chemical Equation Presented).

Iron(II) bromide-catalyzed intramolecular c-h bond amination [1,2]-shift tandem reactions of aryl azides

Nguyen, Quyen,Nguyen, Tuyen,Driver, Tom G.

supporting information, p. 620 - 623 (2013/03/13)

Iron(II) bromide catalyzes the transformation of ortho-substituted aryl azides into 2,3-disubstituted indoles through a tandem ethereal C-H bond amination [1,2]-shift reaction. The preference for the 1,2-shift component of the tandem reaction was established to be Me 1 2 Ph.

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