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Carbamic acid, [2-(methoxymethylamino)-2-oxo-1-[[4-(phenylmethoxy)phenyl]methyl]eth yl]methyl-, 1,1-dimethylethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

876945-79-8

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876945-79-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 876945-79-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,6,9,4 and 5 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 876945-79:
(8*8)+(7*7)+(6*6)+(5*9)+(4*4)+(3*5)+(2*7)+(1*9)=248
248 % 10 = 8
So 876945-79-8 is a valid CAS Registry Number.

876945-79-8Relevant academic research and scientific papers

Naamines and naamidines as novel agents against a plant virus and phytopathogenic fungi

Guo, Pengbin,Li, Gang,Liu, Yuxiu,Lu, Aidang,Wang, Ziwen,Wang, Qingmin

, (2018/09/13)

Naamines, naamidines and various derivatives of these marine natural products were synthesized and characterized by means of nuclear magnetic resonance (NMR) spectroscopy and mass spectrometry. The activities of these alkaloids against a plant virus and phytopathogenic fungi were evaluated for the first time. A benzyloxy naamine derivative 15d displayed excellent in vivo activity against tobacco mosaic virus at 500 μg/mL (inactivation activity, 46%; curative activity, 49%; and protective activity, 41%); its activities were higher than the corresponding activities of the commercial plant virucide ribavirin (32%, 35%, and 34%, respectively), making it a promising new lead compound for antiviral research. In vitro assays revealed that the test compounds exhibited very good antifungal activity against 14 kinds of phytopathogenic fungi. Again, the benzyloxy naamine derivative 15d exhibited broad-spectrum fungicidal activity, emerging as a new lead compound for fungicidal research. Additional in vivo assays indicated that many of the compounds displayed inhibitory effects >30%.

A concise total synthesis of naamidine A

Aberle, Nicholas S.,Lessene, Guillaume,Watson, Keith G.

, p. 419 - 421 (2007/10/03)

A total synthesis of naamidine A is reported. Key benefits of the described pathway include its brevity, its synthetic ease, and its flexibility with respect to the preparation of analogues. Formation of the 2-aminoimidazole core is achieved by condensati

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