19214-08-5 Usage
Uses
Used in Pharmaceutical Research:
Azepan-2-one oxime is used as a key intermediate in the synthesis of pharmaceuticals for various therapeutic purposes. Its unique ability to form complexes with metal ions makes it a valuable component in the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, azepan-2-one oxime is utilized as a building block for the creation of other organic compounds, contributing to the advancement of chemical libraries and the discovery of novel molecules with potential applications.
Used in Coordination Chemistry:
Azepan-2-one oxime functions as a ligand in coordination chemistry, enabling the formation of stable complexes with metal ions. This property is crucial for the study and development of coordination compounds with specific properties and potential uses in various industries.
Used in Medicinal Chemistry:
Azepan-2-one oxime is employed in medicinal chemistry for the development of new drugs. Its potential biological and pharmacological activities are being explored to identify its role in treating various medical conditions.
Overall, azepan-2-one oxime is a multifaceted chemical compound with applications that span across different areas of chemistry and pharmaceutical research, making it an important substance for the development of innovative products and therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 19214-08-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,2,1 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 19214-08:
(7*1)+(6*9)+(5*2)+(4*1)+(3*4)+(2*0)+(1*8)=95
95 % 10 = 5
So 19214-08-5 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N2O/c9-8-6-4-2-1-3-5-7-6/h9H,1-5H2,(H,7,8)
19214-08-5Relevant academic research and scientific papers
Synthesis and Reactions of Cyclic Carbodiimides
Richter, R.,Tucker, B.,Ulrich, H
, p. 1694 - 1700 (2007/10/02)
Modified Tiemann rearrangement on cyclic amidoxime O-methanesulfonates 4 has been used to synthesize cycloalkylene carbodiimides 1 and 4,5,6,7-tetrahydrobenzo-1,3-diazonine (1g). 1,3-Diazacycloocta-1,2-diene (1b), n=5) was also prepared by dehydrosulfuration of pentamethylenethiourea. cycloadducts of the type 20 and 21 are readily formed from 1 as well as 1g with aryl isocyanates and N,N'-diphenylcarbodiimide.Hexafluoroacetone and 1d (n=7) give a dioxazane, 24b (n=7), while 1c (n=6) produces inseparable mixtures of 24a (n=6) and oxazetidine 23. 1,3-Diazacyclohepta-1,2-diene (1a, n=4) oligomerizes on preparation from tetramethylenethiourea, giving predominantly cyclodimer 7 and trimer 8 (not isolated); it can also be trapped with N,N'-diphenylcarbodiimide to give 20a (n=4, X=NC6H5).
Xn:Harmful;
