172090-55-0 Usage
Description
1,4-Dioxa-8-aza-spiro[4.6]undecan-9-one is a unique chemical compound characterized by its spirocyclic structure, which incorporates oxygen and nitrogen heteroatoms. This versatile molecule is recognized for its potential as a precursor in organic synthesis, enabling the preparation of a variety of heterocyclic compounds. Its chemical reactivity and structural attributes make it a promising candidate for applications across different fields, including pharmaceuticals, agrochemicals, and materials science. Furthermore, its spirocyclic framework positions it as a potential chiral building block in asymmetric synthesis, adding to its value in chemical research and industry.
Uses
Used in Pharmaceutical Industry:
1,4-Dioxa-8-aza-spiro[4.6]undecan-9-one is used as a precursor in the synthesis of pharmaceutical compounds due to its ability to form heterocyclic structures, which are often found in biologically active molecules. Its potential as a chiral building block also makes it valuable for the development of enantiomerically pure drugs, enhancing the selectivity and efficacy of pharmaceutical agents.
Used in Agrochemical Industry:
In agrochemicals, 1,4-Dioxa-8-aza-spiro[4.6]undecan-9-one serves as a key intermediate for the creation of novel pesticides and other agrochemical products. Its reactivity and structural features allow for the design of molecules with specific target pest activity, potentially leading to more effective and environmentally friendly agricultural solutions.
Used in Materials Science:
1,4-Dioxa-8-aza-spiro[4.6]undecan-9-one is utilized as a building block in the development of new materials with unique properties. Its incorporation into polymers and other materials can lead to advancements in areas such as high-performance plastics, sensors, and other specialized materials that benefit from its heterocyclic and chiral characteristics.
Used in Organic Synthesis:
As a versatile precursor in organic synthesis, 1,4-Dioxa-8-aza-spiro[4.6]undecan-9-one is used for the preparation of a wide range of heterocyclic compounds. Its ability to participate in various chemical reactions makes it a valuable component in the synthesis of complex organic molecules for research and industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 172090-55-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,0,9 and 0 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 172090-55:
(8*1)+(7*7)+(6*2)+(5*0)+(4*9)+(3*0)+(2*5)+(1*5)=120
120 % 10 = 0
So 172090-55-0 is a valid CAS Registry Number.
172090-55-0Relevant articles and documents
Synthesis and ring-opening polymerization of 5-Azepane-2-one ethylene ketal: A new route to functional aliphatic polyamides
Tarkin-Tas, Eylem,Mathias, Lon J.
, p. 968 - 974 (2010)
A functional derivative of e-caprolactam, 5-azepane-2-one ethylene ketal or y-ethylene ketal e-caprolactam, has been synthesized by a very straightforward and highly efficient Beckmann rearrangement reaction. Homopolymers of this new monomer and its copol
INHIBITORS OF THE HIV INTEGRASE ENZYME
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Page/Page column 72-73, (2010/10/20)
The present invention relates to compounds of formula (I), or a pharmaceutically acceptable salt or solvate thereof, pharmaceutical compositions comprisingm compounds of formula (I), and their methods of use in treating HIV-infected mammals.
Novel Approach to Lactams via (Triisopropylsilyl)azidohydrin Formation and Photoinduced Schmidt Rearrangement
Evans, P. Andrew,Modi, Dilip P.
, p. 6662 - 6663 (2007/10/03)
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