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[(4-Fluorophenyl)(methoxy)methylidene]propanedinitrile is a chemical compound derived from propanedinitrile, featuring a substituted fluorophenyl group and a methoxy group attached to the carbon center. [(4-Fluorophenyl)(methoxy)methylidene]propanedinitrile serves as a building block in the synthesis of other organic compounds and holds potential for various industrial applications.

954221-24-0

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954221-24-0 Usage

Uses

Used in Pharmaceutical Industry:
[(4-Fluorophenyl)(methoxy)methylidene]propanedinitrile is used as a synthetic building block for the development of new pharmaceuticals. Its unique structure allows for the creation of diverse molecules with potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical industry, [(4-Fluorophenyl)(methoxy)methylidene]propanedinitrile is used as a key intermediate in the synthesis of various agrochemicals, such as pesticides and herbicides, due to its versatile chemical structure.
Used in Specialty Chemicals Production:
[(4-Fluorophenyl)(methoxy)methylidene]propanedinitrile is also utilized in the production of specialty chemicals, where its specific properties can be harnessed for applications in materials science, coatings, and other industrial processes.
Safety Note:
It is crucial to handle [(4-Fluorophenyl)(methoxy)methylidene]propanedinitrile with care, as it may pose health and environmental risks. Adhering to safety protocols and using appropriate protective equipment is essential when working with this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 954221-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,4,2,2 and 1 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 954221-24:
(8*9)+(7*5)+(6*4)+(5*2)+(4*2)+(3*1)+(2*2)+(1*4)=160
160 % 10 = 0
So 954221-24-0 is a valid CAS Registry Number.

954221-24-0Relevant academic research and scientific papers

SUBSTITUTED 6-(1H-PYRAZOL-1-YL)PYRIMIDIN-4-AMINE DERIVATIVES AND USES THEREOF

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Page/Page column 166, (2018/04/27)

The present invention covers substituted 6-(1H-pyrazol-1-yl)pyrimidin-4-amine compounds of general formula (I) as described and defined herein, methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions for the treatment or prophylaxis of diseases, in particular for the treatment and/or prophylaxis of cardiovascular and renal diseases, as a sole agent or in combination with other active ingredients.

Studies on the ATP Binding Site of Fyn Kinase for the Identification of New Inhibitors and Their Evaluation as Potential Agents against Tauopathies and Tumors

Tintori, Cristina,La Sala, Giuseppina,Vignaroli, Giulia,Botta, Lorenzo,Fallacara, Anna Lucia,Falchi, Federico,Radi, Marco,Zamperini, Claudio,Dreassi, Elena,Dello Iacono, Lucia,Orioli, Donata,Biamonti, Giuseppe,Garbelli, Mirko,Lossani, Andrea,Gasparrini, Francesca,Tuccinardi, Tiziano,Laurenzana, Ilaria,Angelucci, Adriano,Maga, Giovanni,Schenone, Silvia,Brullo, Chiara,Musumeci, Francesca,Desogus, Andrea,Crespan, Emmanuele,Botta, Maurizio

, p. 4590 - 4609 (2015/06/30)

Fyn is a member of the Src-family of nonreceptor protein-tyrosine kinases. Its abnormal activity has been shown to be related to various human cancers as well as to severe pathologies, such as Alzheimer's and Parkinson's diseases. Herein, a structure-based drug design protocol was employed aimed at identifying novel Fyn inhibitors. Two hits from commercial sources (1, 2) were found active against Fyn with Ki of about 2 μM, while derivative 4a, derived from our internal library, showed a Ki of 0.9 μM. A hit-to-lead optimization effort was then initiated on derivative 4a to improve its potency. Slightly modifications rapidly determine an increase in the binding affinity, with the best inhibitors 4c and 4d having Kis of 70 and 95 nM, respectively. Both compounds were found able to inhibit the phosphorylation of the protein Tau in an Alzheimer's model cell line and showed antiproliferative activities against different cancer cell lines. (Chemical Equation Presented).

Design, synthesis and biological evaluation of 5-amino-1H-pyrazole-4- carboxamide derivatives as potential antitumor agents

Yang, Baowei,Liu, Wukun,Mei, Yicheng,Huang, Dandan,Qian, Hai,Huang, Wenlong,Gust, Ronald

, p. 749 - 755 (2014/07/07)

Adenosine deaminase (ADA) inhibitors have been found to have antitumor activities. Here, thirteen potential adenosine deaminase inhibitors 5-amino-1H-pyrazole-4-carboxamide derivatives were designed, synthesized and screened for antitumor activities. Comp

MODULATION OF PROTEIN TRAFFICKING

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Page/Page column 168, (2009/06/27)

Compounds and compositions are provided for treatment or amelioration of one or more disorders characterized by defects in protein trafficking. A method of treating a disorder characterized by impaired protein trafficking includes administering to a subject or contacting a cell with a compound of Formula I: [formula here] or pharmaceutically acceptable salts or derivatives thereof.

INHIBITION OF ALPHA-SYNUCLEIN TOXICITY

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Page/Page column 71-72, (2008/06/13)

Compounds and compositions are provided for treatment or amelioration of one or more symptoms of α-synuclein toxicity, α-synuclein mediated diseases or diseases in which α-synuclein fibrils are a symptom or cause of the disease.

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