1359658-57-3 Usage
Uses
Used in Pharmaceutical Research:
(S)-2-cyanoMorpholine is used as a building block in the pharmaceutical industry for the synthesis of various drugs and biologically active compounds. Its unique structure allows for the creation of a diverse range of molecules with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, (S)-2-cyanoMorpholine serves as an essential component, facilitating the production of specialty chemicals. Its versatility in chemical reactions makes it a valuable asset for creating complex molecular structures.
Used in Agricultural Industry:
(S)-2-cyanoMorpholine is also utilized as an intermediate in the production of pesticides and agrochemicals. Its incorporation in these products contributes to the development of effective solutions for pest control and crop protection, supporting sustainable agricultural practices.
Used in Academic and Research Settings:
Due to its potential applications and unique chemical properties, (S)-2-cyanoMorpholine is a compound of interest in academic and research settings. It is often employed in the investigation of new chemical reactions, the development of novel synthetic methods, and the exploration of its potential uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 1359658-57-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,9,6,5 and 8 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1359658-57:
(9*1)+(8*3)+(7*5)+(6*9)+(5*6)+(4*5)+(3*8)+(2*5)+(1*7)=213
213 % 10 = 3
So 1359658-57-3 is a valid CAS Registry Number.
1359658-57-3Relevant articles and documents
The synthesis of 2-morpholine carboxylic acid derivatives and their elaboration to 1-aza-4-oxabicyclo[3.3.1]nonan-6-one
King,Martin
, p. 2281 - 2284 (2007/10/19)
Two syntheses of novel 2-morpholine carboxylic acid derivatives are described. The esters were converted into 1-aza-4-oxabicyclo[3.3.1]nonan-6-one, the first example of this ring system, which was further elaborated to the ortho-methoxy benzamide derivative (2).
