40156-53-4 Usage
Molecular structure
A four-membered azetidin-2-one ring attached to a diphenyl group and a substituted phenyl group.
Class
Azetidinone, a class of cyclic amides.
Pharmaceutical applications
Broad range of applications in the pharmaceutical industry.
Derivative
A derivative of 3-phenyl-3-(phenylamino)propanoyl.
Usage
Often used as a building block in organic synthesis for drug discovery and development.
Suitability
Suitable for various pharmacological studies, particularly in the field of medicinal chemistry.
Chemical properties
The specific chemical properties of 1,4-diphenyl-3-[3-phenyl-3-(phenylamino)propanoyl]azetidin-2-one are not provided in the material, but it can be inferred that it has properties typical of azetidinones, such as reactivity and stability in certain conditions.
Structural complexity
The compound is described as complex, indicating a potentially intricate arrangement of atoms and bonds within its molecular structure.
Check Digit Verification of cas no
The CAS Registry Mumber 40156-53-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,1,5 and 6 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 40156-53:
(7*4)+(6*0)+(5*1)+(4*5)+(3*6)+(2*5)+(1*3)=84
84 % 10 = 4
So 40156-53-4 is a valid CAS Registry Number.
40156-53-4Relevant academic research and scientific papers
Synthesis and Stereochemistry of 3-(α-Hydroxybenzyl)-1,4-diphenyl-2-azetidinones
Otto, Hans-Hartwig,Mayrhofer, Roswitha,Bergmann, Hans-Joachim
, p. 1152 - 1161 (2007/10/02)
Aldol reaction between benzaldehydes and 1,4-diphenyl-2-azetidinones 1 catalyzed by lithium diisopropylamide results in formation of the title compound The reactions give satisfactory yields and high diastereoselectivity at three centres in forming the αS
