106973-40-4 Usage
Uses
Used in Medicinal Chemistry:
(S)-Ethyl 4-benzyl-5-oxo-morpholine-3-carboxylate is used as a building block in the synthesis of new pharmaceutical compounds. Its morpholine ring and functional groups, such as the ethyl ester and benzyl group, can be utilized to create novel molecules with potential therapeutic properties.
Used in Drug Development:
(S)-Ethyl 4-benzyl-5-oxo-morpholine-3-carboxylate is used as a starting material or intermediate in the development of new drugs. Its structural features can be modified to optimize pharmacological properties, such as potency, selectivity, and bioavailability, leading to the discovery of new therapeutic agents.
Used in Drug Design:
(S)-Ethyl 4-benzyl-5-oxo-morpholine-3-carboxylate is used as a template in the design of new drugs. Its unique structure can be further modified or combined with other chemical moieties to create new drug candidates with improved pharmacological profiles and therapeutic potential.
Further research may be warranted to determine the specific activities and potential therapeutic applications of (S)-ethyl 4-benzyl-5-oxo-morpholine-3-carboxylate, as its unique structural features and presence in biologically active compounds suggest a promising role in the field of medicinal chemistry and drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 106973-40-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,6,9,7 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 106973-40:
(8*1)+(7*0)+(6*6)+(5*9)+(4*7)+(3*3)+(2*4)+(1*0)=134
134 % 10 = 4
So 106973-40-4 is a valid CAS Registry Number.
InChI:InChI=1/C14H17NO4/c1-2-19-14(17)12-9-18-10-13(16)15(12)8-11-6-4-3-5-7-11/h3-7,12H,2,8-10H2,1H3/t12-/m0/s1
106973-40-4Relevant academic research and scientific papers
Properties and Reactions of Substituted 1,2-Thiazetidine 1,1-Dioxides: Chiral Mono- and Bicyclic 1,2-Thiazetidine 1,1-Dioxides from α-Amino Acids
Meinzer, Alexandra,Breckel, Andrea,Thaher, Bassam Abu,Manicone, Nico,Otto, Hans-Hartwig
, p. 90 - 105 (2007/10/03)
New chiral mono- and bicyclic β-sultams, valuable building blocks for drug synthesis, have been prepared from L-Ala, L-Val, L-Leu, L-Ile, L-Phe, L-Cys, L-Ser, L-Thr, and D-penicillamine by transformation of the COOH group into a methylsulfonyl chloride function, followed by cyclization under basic conditions. Selected properties, derivatives, and reactions of the β-sultams are described.
Chiral Synthesis of 3-Substituted Morpholines via Serine Enantiomers and Reductions of 5-Oxomorpholine-3-carboxylates
Brown, George R.,Foubister, Alan J.,Wright, Brian
, p. 2577 - 2580 (2007/10/02)
The chiral synthesis of 3-hydroxymethyl- and 3-carboxy-morpholines from serine enantiomers is described.Chemoselective and total reductions of 5-oxomorpholine-3-carboxylates are key synthetic steps.
