943026-55-9 Usage
Description
(4-(prop-2-yn-1-yloxy)phenyl)methanamine is a chemical compound that belongs to the class of amines, which are organic compounds containing a basic nitrogen atom with a lone pair. It features a phenyl group with a prop-2-yn-1-yloxy substituent attached to it, as well as a methanamine functional group. This versatile compound is widely used in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals due to its unique chemical structure.
Uses
Used in Pharmaceutical Industry:
(4-(prop-2-yn-1-yloxy)phenyl)methanamine is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the creation of complex organic molecules that can be tailored for specific medical applications, making it a valuable asset in drug development.
Used in Agrochemical Industry:
In the agrochemical industry, (4-(prop-2-yn-1-yloxy)phenyl)methanamine is utilized as a key component in the production of various agrochemicals. Its chemical properties enable the development of compounds that can be used in the creation of pesticides, herbicides, and other agricultural products to improve crop yield and protect against pests.
Used in Chemical Research:
(4-(prop-2-yn-1-yloxy)phenyl)methanamine serves as a reagent in chemical research, where its unique structure can be exploited to study various chemical reactions and mechanisms. This contributes to the advancement of scientific knowledge and the development of new chemical processes.
Used in Material Science:
(4-(prop-2-yn-1-yloxy)phenyl)methanamine is also used in the development of new materials, taking advantage of its versatile chemical structure. It can be incorporated into the synthesis of advanced materials with specific properties, such as improved strength, durability, or chemical resistance, for use in various industries.
Overall, (4-(prop-2-yn-1-yloxy)phenyl)methanamine is a multifaceted compound with a wide range of applications across different industries, making it an important tool in the fields of pharmaceuticals, agrochemicals, chemical research, and material science.
Check Digit Verification of cas no
The CAS Registry Mumber 943026-55-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,3,0,2 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 943026-55:
(8*9)+(7*4)+(6*3)+(5*0)+(4*2)+(3*6)+(2*5)+(1*5)=159
159 % 10 = 9
So 943026-55-9 is a valid CAS Registry Number.
943026-55-9Relevant articles and documents
Multitasking with Chemical Fuel: Dissipative Formation of a Pseudorotaxane Rotor from Five Distinct Components
Ghosh, Amit,Paul, Indrajit,Schmittel, Michael
, p. 5319 - 5323 (2021/05/04)
A 3-fold completive self-sorted library of dynamic motifs was integrated into the design of the pseudorotaxane-based rotor [Zn(2·H+)(3)(4)]2+ operating at k298 = 15.4 kHz. The rotational motion in the five-component device is based on association/dissocia
Radiolabeled Selective Matrix Metalloproteinase 13 (MMP-13) Inhibitors: (Radio)Syntheses and in Vitro and First in Vivo Evaluation
Hugenberg, Verena,Wagner, Stefan,Kopka, Klaus,Sch?fers, Michael,Schuit, Robert C.,Windhorst, Albert D.,Hermann, Sven
, p. 307 - 321 (2017/04/26)
The noninvasive imaging of MMP activity in vivo could have a high impact in basic research as well as in clinical applications. This approach can be established using radiolabeled MMP inhibitors (MMPIs) as tracers for the detection of activated MMPs by means of PET. However, the complexity of diseases associated with dysregulated MMP expression necessitates the imaging of distinct MMPs or MMP subgroups to distinguish their individual role in specific diseases. To this end, selective and potent MMP-13 inhibitors based on a N,N′-bis(benzyl)pyrimidine-4,6-dicarboxamide core have been synthesized and successfully radiolabeled with carbon-11, fluorine-18, and gallium-68. Selected radiolabeled candidates were evaluated in vitro and in vivo regarding their pharmacokinetic properties and metabolic stability.
A Fluorescent and Switchable Rotaxane Dual Organocatalyst
Kwan, Chak-Shing,Chan, Albert S. C.,Leung, Ken Cham-Fai
, p. 976 - 979 (2016/03/15)
Rotaxane organocatalysis presents a new direction toward controlled one-pot catalytic reactions. By combining molecular switches and catalysts, fluorescence and pH-responsive switching along with the exclusive selectivity of dual catalytic reactions are d
