276252-73-4 Usage
Description
Morpholine, 2,6-dimethyl-, (2S,6S)is an organic compound characterized by its unique molecular structure, featuring a morpholine ring with two methyl groups attached at the 2nd and 6th positions. Morpholine, 2,6-dimethyl-, (2S,6S)is known for its specific stereochemistry, with the (2S,6S)configuration, which plays a crucial role in its reactivity and potential applications.
Uses
Used in Pharmaceutical Industry:
Morpholine, 2,6-dimethyl-, (2S,6S)is used as a synthetic intermediate for the development of BIRB 796 analogs, which are designed for the treatment of autoimmune diseases. These analogs possess p38α kinase-inhibiting activities, making them valuable in modulating the immune response and providing therapeutic benefits for patients suffering from autoimmune conditions.
Used in Chemical Research:
Morpholine, 2,6-dimethyl-, (2S,6S)is also utilized in the synthesis of chromium aminocarbene complexes of diterpenoids. These complexes are of interest to researchers due to their potential applications in various fields, including catalysis and material science. The unique properties of the (2S,6S)Morpholine, 2,6-dimethyl-, make it a valuable building block in the development of novel compounds with specific functionalities.
Check Digit Verification of cas no
The CAS Registry Mumber 276252-73-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,6,2,5 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 276252-73:
(8*2)+(7*7)+(6*6)+(5*2)+(4*5)+(3*2)+(2*7)+(1*3)=154
154 % 10 = 4
So 276252-73-4 is a valid CAS Registry Number.
276252-73-4Relevant 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.
