153783-23-4 Usage
Uses
Used in Pharmaceutical Synthesis:
(S)-5-Ethoxycarbonyl-2-phenyl-Δ1-pyrroline is used as a starting material for the synthesis of various pharmaceuticals and biologically active molecules. Its unique structure and reactivity contribute to the development of new drugs and therapeutic agents.
Used in Drug Discovery and Development:
In the field of drug discovery and development, (S)-5-Ethoxycarbonyl-2-phenyl-Δ1-pyrroline serves as a key component in the design and synthesis of novel compounds with potential medicinal properties. Its versatility allows for the exploration of various chemical pathways and the creation of innovative drug candidates.
Used in Organic Synthesis as a Ligand:
(S)-5-Ethoxycarbonyl-2-phenyl-Δ1-pyrroline also has potential applications as a ligand for catalytic processes in organic synthesis. Its distinct characteristics enable it to facilitate and enhance the efficiency of certain chemical reactions, making it an important molecule in the field of synthetic chemistry.
Used in Chemical Research:
In addition to its practical applications, (S)-5-Ethoxycarbonyl-2-phenyl-Δ1-pyrroline is also utilized in chemical research to study the properties and behavior of chiral molecules. Understanding the interactions and reactions of (S)-5-Ethoxycarbonyl-2-phenyl-Δ1-pyrroline can provide valuable insights into the broader field of chemistry and contribute to the advancement of scientific knowledge.
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 academic research and scientific papers
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
Convenient synthesis of C-aza-2,3-dideoxynucleosides
Momotake, Atsuya,Togo, Hideo,Yokoyama, Masataka
, p. 1193 - 1200 (2007/10/03)
l-Aryl-l,2,3,4-tetradeoxy-l,4-imino-D-pentitols 5 and 9f are easily synthesized from TV-Boc-L-pyroglutamate 1 via a successive procedure involving regioselective ring-opening, recyclization with dehydration, stereoselective reduction, and reduction of the
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
General method for the synthesis of 5-arylpyrrole-2-carboxylic acids
Ezquerra, Jesus,Pedregal, Concepcion,Rubio, Almudena,Valenciano, Jesus,Garcia Navio, Jose Luis,Alvarez-Builla, Julio,Vaquero, Juan Jose
, p. 6317 - 6320 (2007/10/02)
5-Arylpyrrole-2-carboxylic acids are prepared by DDQ oxidative aromatization of the corresponding ethyl 2-aryl-Δ1-pyrroline-5-carboxylate followed by basic hydrolysis.
