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(2R,3S)-2,3-diphenylmorpholine is a morpholine derivative, an organic compound characterized by a unique molecular structure featuring a morpholine ring with two phenyl groups attached. (2R,3S)-2,3-diphenylmorpholine is known for its potential applications in pharmaceuticals, material science, and organic synthesis.

23204-68-4

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23204-68-4 Usage

Uses

Used in Pharmaceutical Industry:
(2R,3S)-2,3-diphenylmorpholine is used as a building block in the synthesis of complex molecules for pharmaceutical applications due to its unique molecular structure and potential pharmacological activities.
Used in Material Science:
(2R,3S)-2,3-diphenylmorpholine is utilized in material science for its potential to contribute to the development of new materials with specific properties, leveraging its structural characteristics.
Used in Organic Synthesis:
(2R,3S)-2,3-diphenylmorpholine is employed as an intermediate in organic synthesis, facilitating the creation of a variety of organic compounds for research and industrial purposes.
Used in Drug Development:
(2R,3S)-2,3-diphenylmorpholine is studied for its potential use in the development of new drugs, showing promise in various research areas, particularly for its potential pharmacological properties.

Check Digit Verification of cas no

The CAS Registry Mumber 23204-68-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,2,0 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 23204-68:
(7*2)+(6*3)+(5*2)+(4*0)+(3*4)+(2*6)+(1*8)=74
74 % 10 = 4
So 23204-68-4 is a valid CAS Registry Number.

23204-68-4Relevant academic research and scientific papers

An improved synthesis and resolution of cis- and trans-2,3-diphenyl morpholines

Jagtap, Ravindra S.,Joshi, Navalkishore N.

, p. 1861 - 1864 (2012/01/13)

An improved procedure for the synthesis of cis- and trans-2,3-diphenyl morpholines with good overall yield is described. The stereoisomers were efficiently resolved through the corresponding diastereomeric salts using tartaric acid and (R)-mandelic acid.

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