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1261352-75-3

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1261352-75-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1261352-75-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,1,3,5 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1261352-75:
(9*1)+(8*2)+(7*6)+(6*1)+(5*3)+(4*5)+(3*2)+(2*7)+(1*5)=133
133 % 10 = 3
So 1261352-75-3 is a valid CAS Registry Number.

1261352-75-3Relevant academic research and scientific papers

Synthesis and biological evaluation of chalcone derivatives containing aminoguanidine or acylhydrazone moieties

Wei, Zhi-Yu,Chi, Ke-Qiang,Yu, Zhan-Kui,Liu, Hong-Yan,Sun, Liang-Peng,Zheng, Chang-Ji,Piao, Hu-Ri

supporting information, p. 5920 - 5925 (2016/12/06)

Three novel series of chalcone derivatives containing an aminoguanidine or acylhydrazone moiety were designed, synthesized and evaluated in terms of their antibacterial, antifungal and anti-inflammatory activities. Most of the synthesized compounds showed

Synthesis and antimicrobial evaluation of L-phenylalanine-derived C5-substituted rhodanine and chalcone derivatives containing thiobarbituric acid or 2-thioxo-4-thiazolidinone

Zheng, Chang-Ji,Song, Ming-Xia,Wu, Yan,Sun, Liang-Peng,Li, Yin-Jing,Piao, Hu-Ri,Jin, Xin,Yu, Li-Jun

, p. 203 - 209,7 (2012/12/12)

Four novel series of compounds, including the l-phenylalanine-derived C5-substituted rhodanine (6a-q, 7a-j) and chalcone derivatives containing thiobarbituric acid or 2-thioxo-4-thiazolidinone (9a-e, 11a-e) have been designed, synthesized, characterized, and evaluated for their antibacterial activity. Some of these compounds showed significant antibacterial activity against Gram-positive bacterias, especially against the strains of multidrug-resistant clinical isolates, among which compounds 6c-e, 6g, 6i, 6j and 6q exhibiting high levels of antimicrobial activity against Staphylococcus aureus RN4220 with minimum inhibitory concentration (MIC) values of 2 μg/mL. Compound 6q showed the most potent activity of all of the compounds against all of the test multidrug-resistant clinical isolates tested. Unfortunately, however, none of the compounds were active against Gram-negative bacteria at 64 μg/mL.

Synthesis of new chalcone derivatives containing a rhodanine-3-acetic acid moiety with potential anti-bacterial activity

Chen, Zhen-Hua,Zheng, Chang-Ji,Sun, Liang-Peng,Piao, Hu-Ri

scheme or table, p. 5739 - 5743 (2011/02/23)

With an intention to synergize the anti-bacterial activity of chalcones and rhodanine-3-acetic acid, several hybrid compounds possessing chalcone and rhodanine-3-acetic acid moieties were synthesized and tested for their anti-bacterial activity. Some comp

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