56414-76-7 Usage
Uses
Used in Organic Synthesis:
(2-Morpholin-4-yl-2-oxo-ethyl)-carbamic acid benzyl ester serves as a valuable chemical intermediate in organic synthesis, facilitating the creation of a range of complex organic molecules. Its unique structural features contribute to its reactivity and utility in forming diverse chemical products.
Used in Pharmaceutical Production:
In the pharmaceutical industry, (2-Morpholin-4-yl-2-oxo-ethyl)-carbamic acid benzyl ester is utilized as a chemical intermediate for the development of new drugs. Its structural components, including the morpholine ring and carbamic acid group, may be integral in the synthesis of medicinal compounds with specific therapeutic properties.
Used in Agrochemical Development:
Similarly, in agrochemicals, (2-Morpholin-4-yl-2-oxo-ethyl)-carbamic acid benzyl ester plays a role as an intermediate in the synthesis of pesticides, herbicides, or other agricultural chemicals. Its potential to form stable and bioactive molecules makes it a candidate for enhancing crop protection and yield.
Further research is essential to explore the specific applications and optimize the synthesis processes of (2-Morpholin-4-yl-2-oxo-ethyl)-carbamic acid benzyl ester, ensuring its safe and effective use across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 56414-76-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,4,1 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 56414-76:
(7*5)+(6*6)+(5*4)+(4*1)+(3*4)+(2*7)+(1*6)=127
127 % 10 = 7
So 56414-76-7 is a valid CAS Registry Number.
56414-76-7Relevant academic research and scientific papers
Generation of Oxyphosphonium Ions by Photoredox/Cobaloxime Catalysis for Scalable Amide and Peptide Synthesis in Batch and Continuous-Flow
Chen, Xiangyang,Houk, Kendall N.,Mo, Jia-Nan,Su, Junqi,Umanzor, Alexander,Zhang, Zheng,Zhao, Jiannan
supporting information, (2022/01/06)
Phosphine-mediated deoxygenative nucleophilic substitutions, such as the Mitsunobu reaction, are of great importance in organic synthesis. However, the conventional protocols require stoichiometric oxidants to trigger the formation of the oxyphosphonium i
Enol esters as intermediates for the facile conversion of amino acids into amides and dipeptides
Kabouche,Bruneau,Dixneuf
, p. 5359 - 5362 (2007/10/02)
N-Protected amino enol esters are easily transformed at room temperature into amino amides, and in the presence of potassium cyanide as catalyst, into tertiary amides and dipeptides.
