153783-23-4 Usage
General Description
(S)-5-Ethoxycarbonyl-2-phenyl-Δ1-pyrroline is a chemical compound that belongs to the class of pyrrolines. It is a chiral molecule, meaning it has a non-superimposable mirror image, and the (S)-enantiomer is the specific form being described. (S)-5-Ethoxycarbonyl-2-phenyl-Δ1-pyrroline is commonly used in organic chemistry as a starting material for the synthesis of various pharmaceuticals and biologically active molecules. Its unique structure and reactivity make it a valuable building block in the creation of complex organic compounds, and it has applications in drug discovery and development. Moreover, it has potential as a ligand for catalytic processes in organic synthesis. Its distinct characteristics and versatile applications make it an important molecule in the field of synthetic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 153783-23-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,7,8 and 3 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 153783-23:
(8*1)+(7*5)+(6*3)+(5*7)+(4*8)+(3*3)+(2*2)+(1*3)=144
144 % 10 = 4
So 153783-23-4 is a valid CAS Registry Number.
153783-23-4Relevant articles and documents
Asymmetric conjugate addition of glycine derivatives under copper catalysis
Strohmeier, Mark,Leach, Kevin,Zajac, Matthew A.
supporting information; experimental part, p. 12335 - 12338 (2012/02/01)
Coppertunity knocks: An inexpensive, practical, and environmentally benign procedure for the enantioselective addition of glycine derivatives to α,β-unsaturated ketones has been developed (see scheme). By modifying the workup, the conjugate addition produ
Design of orally active dual inhibitors of neutral endopeptidase and angiotensin-converting enzyme with long duration of action
Fournie-Zaluski, Marie-Claude,Coric, Pascale,Thery, Vincent,Gonzalez, Walter,Meudal, Hervé,Turcaud, Serge,Michel, Jean-Baptiste,Roques, Bernard P.
, p. 2594 - 2608 (2007/10/03)
Mercaptoacyl dipeptides, containing a glycine linked to a C-terminal 5- phenylproline, have been synthesized in order to obtain new highly efficient dual inhibitors of the two zinc metallopeptidases, neutral endopeptidase (NEP) and angiotensin-converting
