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1H-Isoindole-1,3(2H)-dione, 2-(4-mercaptophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

72650-24-9

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72650-24-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 72650-24-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,2,6,5 and 0 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 72650-24:
(7*7)+(6*2)+(5*6)+(4*5)+(3*0)+(2*2)+(1*4)=119
119 % 10 = 9
So 72650-24-9 is a valid CAS Registry Number.

72650-24-9Relevant academic research and scientific papers

A phthalimidation protocol that follows protein defined parameters

Singudas, Rohith,Adusumalli, Srinivasa Rao,Joshi, Pralhad Namdev,Rai, Vishal

, p. 473 - 476 (2015)

This work outlines the first phthalimidation protocol suitable for protein labeling and performed in aqueous media at room temperature and neutral pH with no catalyst or co-reagent required. The methodology is suitable for a range of amines and its efficiency was determined with chemoselective and site-selective protein labeling. This journal is

Synthesis, antiproliferative, and antimicrobial properties of novel phthalimide derivatives

Chi, Chun-Lan,Xu, Lu,Li, Jun-Jie,Liu, Yang,Chen, Bao-Quan

, p. 120 - 131 (2021/11/30)

In this research, a series of new phthalimide derivatives with disulfide bonds were designed and synthesized, and their in vitro antiproliferative activities against normal cell lines L929, human cancer cells Hela, MCF-7, and A549 were assessed via the CCK-8 assay. At the same time, in vitro antimicrobial activities of all compounds were evaluated against Gram-negative Escherichia coli and Gram-positive Staphylococcus aureus. The preliminary bioassay results showed that a series of derivatives of phthalimide 6a–e, 7a–e, 8a–e, and 9a–e exhibited different degrees of antiproliferative activity, and some compounds revealed higher antiproliferative effects than the positive control 5-fluorouracil. Compound 9b (IC50 = 2.86 μM) exhibited the best proliferation inhibitory activities against A549 cells. It is shown that compounds 6b (IC50 = 2.94 μM) and 6c (IC50 = 3.20 μM) exhibited excellent biological activities against Hela cells. Compound 9b (IC50 = 3.21 μM) displayed the highest antitumor activities against MCF-7 cells. In addition, most of the target compounds had relatively low cytotoxicities against the normal cell line L929. The biological results indicated that all the tested compounds possessed antimicrobial activity with certain degrees against E. coli and S. aureus. [Figure not available: see fulltext.]

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