146117-93-3 Usage
Uses
Used in Pharmaceutical Industry:
(PIPERIDIN-4-YLOXY)-ACETIC ACID is used as a building block for the development of pharmaceutical drugs due to its ability to contribute to the creation of complex molecular structures with potential therapeutic effects.
Used in Agrochemical Industry:
In agrochemicals, (PIPERIDIN-4-YLOXY)-ACETIC ACID is utilized as a precursor in the synthesis of compounds that can have applications in crop protection and other agricultural chemical products, leveraging its structural properties to enhance the effectiveness of these compounds.
Used in Materials Science:
(PIPERIDIN-4-YLOXY)-ACETIC ACID is employed as a component in the development of new materials, where its chemical structure can influence the properties of the resulting materials, such as their reactivity, stability, or other physical characteristics.
Used in Organic Synthesis:
As a versatile building block in organic synthesis, (PIPERIDIN-4-YLOXY)-ACETIC ACID is used for creating a wide array of complex chemical structures that can be applied in various chemical and industrial processes, capitalizing on its unique structural features to facilitate the formation of desired products.
Check Digit Verification of cas no
The CAS Registry Mumber 146117-93-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,1,1 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 146117-93:
(8*1)+(7*4)+(6*6)+(5*1)+(4*1)+(3*7)+(2*9)+(1*3)=123
123 % 10 = 3
So 146117-93-3 is a valid CAS Registry Number.
146117-93-3Relevant academic research and scientific papers
Acetic acid derivatives
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, (2008/06/13)
Acetic acid derivatives of the formula STR1 wherein L, M, T and Q have the significance given in the description, can be used for the treatment or prophylaxis of illnesses which are caused by the binding of adhesive proteins to blood platelets and by blood platelet aggregation and cell-cell adhesion, and are manufactured by cleaving protecting groups in the corresponding protected compounds or by converting the cyano group into the amidino group in corresponding nitriles.
