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BenzenaMine, 4-[(4-nitrophenyl)Methoxy]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25464-96-4

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25464-96-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25464-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,6 and 4 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25464-96:
(7*2)+(6*5)+(5*4)+(4*6)+(3*4)+(2*9)+(1*6)=124
124 % 10 = 4
So 25464-96-4 is a valid CAS Registry Number.

25464-96-4Downstream Products

25464-96-4Relevant academic research and scientific papers

Discovery of 2-((4,6-dimethylpyrimidin-2-yl)thio)-N-phenylacetamide derivatives as new potent and selective human sirtuin 2 inhibitors

Yang, Lingling,Ma, Xiaobo,Yuan, Chen,He, Yanying,Li, Ling,Fang, Sha,Xia, Wei,He, Tao,Qian, Shan,Xu, Zhihong,Li, Guobo,Wang, Zhouyu

, p. 230 - 241 (2017/04/19)

Human sirtuin 2 (SIRT2) plays pivotal roles in multiple biological processes such as cell cycle regulation, autophagy, immune and inflammatory responses. Dysregulation of SIRT2 was considered as a main aspect contributing to several human diseases, including cancer. Development of new potent and selective SIRT2 inhibitors is currently desirable, which may provide a new strategy for treatment of related diseases. Herein, a structure-based optimization approach led to new 2-((4,6-dimethylpyrimidin-2-yl)thio)-N-phenylacetamide derivatives as SIRT2 inhibitors. SAR analyses with new synthesized derivatives revealed a number of new potent SIRT2 inhibitors, among which 28e is the most potent inhibitor with an IC50 value of 42?nM. The selectivity analyses found that 28e has a very good selectivity to SIRT2 over SIRT1 and SIRT3. In cellular assays, 28e showed a potent ability to inhibit human breast cancer cell line MCF-7 and increase the acetylation of α-tubulin in a dose-dependent manner. This study will aid further efforts to develop highly potent and selective SIRT2 inhibitors for the treatment of cancer and other related diseases.

Direct synthesis of anilines and nitrosobenzenes from phenols

St Amant,Frazier,Newmeyer,Fruehauf,Read De Alaniz

, p. 5520 - 5524 (2016/07/06)

A one-pot synthesis of anilines and nitrosobenzenes from phenols has been developed using an ipso-oxidative aromatic substitution (iSOAr) process. The products are obtained in good yields under mild and metal-free conditions. The leaving group effect on reactions that proceed through mixed quionone monoketals has also been investigated and a predictive model has been established.

Synthesis and antimicrobial activity of some new aminomethylated benzazoles

Rastogi, Nisheeth,Kant, Padam

, p. 77 - 80 (2019/01/21)

A new series of aminomethylated benzazoles has been synthesized by the reaction of benzazoles with 4-(4-nitrobenzyloxy)-aniline in the presence of formaldehyde and screened for antimicrobial potential against human pathogenic fungi and bacteria. The struc

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