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2-(2-methoxy-2-oxoethyl)phenyl 2-(3,4-diethoxyphenyl)acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1104307-63-2

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1104307-63-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1104307-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,4,3,0 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1104307-63:
(9*1)+(8*1)+(7*0)+(6*4)+(5*3)+(4*0)+(3*7)+(2*6)+(1*3)=92
92 % 10 = 2
So 1104307-63-2 is a valid CAS Registry Number.

1104307-63-2Downstream Products

1104307-63-2Relevant academic research and scientific papers

Synthesis, characterization and structure-activity relationship analysis of novel depsides as potential antibacterials

Lv, Peng-Cheng,Xiao, Zhu-Ping,Fang, Rui-Qin,Li, Huan-Qiu,Zhu, Hai-Liang,Liu, Chang-Hong

experimental part, p. 1779 - 1787 (2009/05/26)

Twenty-six depsides were synthesized to screen for their antibacterial activity. All of them were reported for the first time. Their chemical structures were clearly determined by 1H NMR, 13C NMR, ESI mass spectra and elemental analyses, coupled with one selected single-crystal structure. All the compounds were assayed for antibacterial activities against three Gram-positive bacterial strains (Bacillus subtilis ATCC 6633, Staphylococcus aureus ATCC 6538 and Streptococcus faecalis ATCC 9790) and three Gram-negative bacterial strains (Escherichia coli ATCC 35218, Pseudomonas aeruginosa ATCC 13525 and Enterobacter cloacae ATCC 13047) by MTT method. Compound 2-(2-methoxy-2-oxoethyl)phenyl 3-nitrobenzoate (C10) and 2-(2-ethoxy-2-oxoethyl)phenyl 3-nitrobenzoate (C23) showed powerful antibacterial activities against B. subtilis with MIC of 0.78 μg/mL while compound 2-(2-methoxy-2-oxoethyl)phenyl 2-(3,4-diethoxyphenyl)acetate (C8) and 2-(2-ethoxy-2-oxoethyl)phenyl 2-(3,4-diethoxyphenyl)acetate (C21) exhibited significant antibacterial activities against E. coli with MIC of 1.562 μg/mL, which were superior to the positive controls penicillin G and kanamycin B, respectively. On the basis of the biological results, structure-activity relationships were discussed.

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