61108-69-8 Usage
Uses
Used in Pharmaceutical Development:
1,4-oxazepan-3-one is used as a key intermediate in the synthesis of various biologically active compounds. Its versatile reactivity allows for the creation of a wide range of pharmaceutical agents with diverse therapeutic properties.
Used in Organic Synthesis:
1,4-oxazepan-3-one serves as a valuable building block in organic synthesis, enabling the development of complex organic molecules with potential applications in various industries.
Used in Drug Discovery:
Due to its interesting pharmacological properties, such as sedative and anxiolytic effects, 1,4-oxazepan-3-one is used as a potential candidate for drug discovery. Its unique structure and reactivity contribute to the development of new therapeutic agents with novel mechanisms of action.
Used in Research:
1,4-oxazepan-3-one is utilized in research settings to explore its potential applications and to gain a deeper understanding of its chemical properties and reactivity. This knowledge can be applied to the development of new synthetic methods and the discovery of new compounds with therapeutic potential.
Check Digit Verification of cas no
The CAS Registry Mumber 61108-69-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,1,0 and 8 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 61108-69:
(7*6)+(6*1)+(5*1)+(4*0)+(3*8)+(2*6)+(1*9)=98
98 % 10 = 8
So 61108-69-8 is a valid CAS Registry Number.
InChI:InChI=1/C5H9NO2/c7-5-4-8-3-1-2-6-5/h1-4H2,(H,6,7)
61108-69-8Relevant academic research and scientific papers
ANTIPROLIFERATION COMPOUNDS AND USES THEREOF
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Paragraph 1154, (2019/11/11)
The present invention provides compounds of Formula I′, or pharmaceutically acceptable salts thereof, pharmaceutical compositions thereof, and methods of use thereof for treating cellular proliferative disorders (e.g., cancer).
Synthesis of analogs of (1,4)-3- and 5-imino oxazepane, thiazepane, and diazepane as inhibitors of nitric oxide synthases
Shankaran,Donnelly, Karla L.,Shah, Shrenik K.,Caldwell, Charles G.,Chen, Ping,Hagmann, William K.,MacCoss, Malcolm,Humes, John L.,Pacholok, Stephen G.,Kelly, Theresa M.,Grant, Stephan K.,Wong, Kenny K.
, p. 5907 - 5911 (2007/10/03)
The preparation and SAR of a series of iNOS inhibitors leading to the most potent compound, incorporating a (1,4)-5-imino thiazepane (R = n-Pr) is disclosed. A series of 3- and 5-imino analogs from oxazepane, thiazepane, and diazepane was prepared and eva
Oxacaprolactams
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, (2008/06/13)
3-OXACAPROLACTAM IS PREPARED BY A PROCESS WHICH COMPRISES: CONTACTING AN ORGANIC ACID ANHYDRIDE SOLUTION OF A CYANOALKOXYALKANOATE WITH HYDROGEN IN THE PRESENCE OF A NOBLE METAL HYDROGENATION CATALYST TO PREPARE AN AMIDE-ESTER; AND HEATING THE AMIDE-ESTER IN EXCESS WATER AT A TEMPERATURE ABOVE ABOUT 200° C.
