297172-01-1 Usage
Uses
Used in Pharmaceutical Synthesis:
(R)-ethyl 3-Methylpiperidine-3-carboxylate is used as an intermediate or building block for the synthesis of various pharmaceuticals. Its unique structure and chirality make it a valuable component in the development of new drugs and medications.
Used in Organic Compounds Synthesis:
(R)-ethyl 3-Methylpiperidine-3-carboxylate is also utilized in the synthesis of organic compounds, contributing to the creation of a wide range of chemical products with diverse applications.
Used in Chemical Research and Development:
(R)-ethyl 3-Methylpiperidine-3-carboxylate plays a role in chemical research and development, where it can be employed to study and understand the properties and reactions of chiral molecules, potentially leading to advancements in various fields of chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 297172-01-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,7,1,7 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 297172-01:
(8*2)+(7*9)+(6*7)+(5*1)+(4*7)+(3*2)+(2*0)+(1*1)=161
161 % 10 = 1
So 297172-01-1 is a valid CAS Registry Number.
297172-01-1Relevant academic research and scientific papers
Synthesis of a potent hNK-1 receptor antagonist via an SN2 reaction of an enantiomerically pure α-alkoxy sulfonate
Nelson, Todd D.,Rosen, Jonathan D.,Smitrovich, Jacqueline H.,Payack, Joseph,Craig, Bridgette,Matty, Louis,Huffman, Mark A.,McNamara, James
, p. 55 - 58 (2007/10/03)
(Chemical Equation Presented) The concise synthesis of a stereochemically rich hNK-1 receptor antagonist is described. The synthesis is highlighted by an SN2 reaction of an enantiomerically pure α-alkoxy sulfonate (orthogonally protected butane triol), which was prepared by utilizing salen-mediated hydrolytic kinetic resolution technology. A stereocontrolled acetalization was employed to connect two enantiomerically pure fragments with a high degree of diastereoselectivity.
