127958-64-9 Usage
Description
Hexahydro-2H-benzo[b][1,4]oxazin-3(4H)-one, also known as morpholin-3-one, is a heterocyclic organic compound with the molecular formula C7H11NO2. It features a six-membered ring containing oxygen and nitrogen atoms, and is widely recognized for its applications in organic synthesis and pharmaceuticals. Hexahydro-2H-benzo[b][1,4]oxazin-3(4H)-one serves as a versatile building block in the production of various drugs and pharmaceutical compounds, highlighting its significance in the field of organic chemistry and pharmaceuticals.
Uses
Used in Pharmaceutical Industry:
Hexahydro-2H-benzo[b][1,4]oxazin-3(4H)-one is used as an intermediate in the synthesis of various drugs for its ability to contribute to the formation of complex molecular structures. Its unique structure and properties make it a valuable component in the development of new pharmaceuticals.
Used in Organic Synthesis:
In the realm of organic synthesis, Hexahydro-2H-benzo[b][1,4]oxazin-3(4H)-one is utilized as a key building block, enabling the creation of a diverse array of chemical compounds. Its presence in reactions can lead to the production of molecules with specific therapeutic or functional properties.
Used in Chemical Reactions and Processes:
Due to its distinctive structural features, Hexahydro-2H-benzo[b][1,4]oxazin-3(4H)-one is also employed in various chemical reactions and processes. It plays a crucial role in facilitating specific transformations and the synthesis of target molecules, further expanding its utility in the chemical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 127958-64-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,9,5 and 8 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 127958-64:
(8*1)+(7*2)+(6*7)+(5*9)+(4*5)+(3*8)+(2*6)+(1*4)=169
169 % 10 = 9
So 127958-64-9 is a valid CAS Registry Number.
127958-64-9Relevant articles and documents
A concise and efficient synthesis of substituted morpholines
Dugar, Sundeep,Sharma, Amit,Kuila, Bilash,Mahajan, Dinesh,Dwivedi, Sandeep,Tripathi, Vinayak
, (2015/02/19)
A simple and efficient method has been developed for the synthesis of substituted morpholines by a sequence of coupling, cyclization, and reduction reactions of easily available amino alcohols and α-halo acid chlorides. Various mono-, di-, and trisubstituted morpholines, spiro morpholines, and ring-fused morpholines, as well as morpholine homologues, were synthesized in good to excellent yields by a single methodology under similar reaction conditions. The method was also used in a multigram synthesis of (3S)-3-methylmorpholine.
Preparation of diastereomerically pure immunologically active carbocyclic nor-muramyldipeptide analogues
Kikelj,Kidric,Pristovisek,Pecar,Urleb,Krbavcic,Honig
, p. 5915 - 5932 (2007/10/02)
The preparation of diastereomerically pure immunologically active carbocyclic nor-muramyldipeptide analogues (1'R,2'R)-/(1'S,2'S)-N-[2-(2'-acetylaminocyclohexyloxy)acetyl]-L- alanyl-D-isoglutamine and (1'R,2'R)-/(1'S,2'S)-N-[2-(2'-acetylaminocyclohexyloxy)acetyl]-L- alanyl-D-glutamic acid is described. The title compounds were synthesized using two independent synthetic routes from racemic trans-2-azidocyclohexanol and (1R,2R)-/(1S,2S)-2-aminocyclohexanol, respectively.
