89451-58-1 Usage
Uses
Used in Pharmaceutical Industry:
(2S,4S)-2-Methylpiperidin-4-ol is used as an intermediate in the synthesis of pharmaceuticals for its specific stereochemistry, which is crucial in the production of certain drugs and other organic compounds. Its unique properties allow for the development of new therapeutic agents with potentially beneficial effects.
Used in Agrochemical Industry:
In the agrochemical sector, (2S,4S)-2-Methylpiperidin-4-ol serves as an intermediate in the synthesis of agrochemicals, contributing to the development of effective and targeted pest control solutions.
Used in Research and Development:
(2S,4S)-2-Methylpiperidin-4-ol is utilized as a building block in research and development for creating new molecules with potentially beneficial properties, expanding the scope of chemical and pharmaceutical innovation.
Used in Medicinal Chemistry:
(2S,4S)-2-Methylpiperidin-4-ol may have potential applications in the field of medicinal chemistry, where it can be employed in the development of new therapeutic agents, leveraging its unique stereochemistry to enhance the efficacy and selectivity of drug candidates.
Check Digit Verification of cas no
The CAS Registry Mumber 89451-58-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,4,5 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 89451-58:
(7*8)+(6*9)+(5*4)+(4*5)+(3*1)+(2*5)+(1*8)=171
171 % 10 = 1
So 89451-58-1 is a valid CAS Registry Number.
89451-58-1Relevant academic research and scientific papers
Diastereoselective synthesis of new zwitterionic bicyclic lactams, scaffolds for construction of 2-substituted-4-hydroxy piperidine and its pipecolic acid derivatives
Aparicio, David M.,Bernès, Sylvain,Gnecco, Dino,Juárez, Jorge R.,Orea, María L.,Reyes-Bravo, Enrique,Terán, Joel L.
, p. 4187 - 4190 (2022/02/16)
The synthesis of new chiral highly functionalized zwitterionic bicyclic lactams starting from acyclic β-enaminoesters derived from (R)-(-)-2-phenylglycinol is described. The key step involved an intramolecular non-classical Corey-Chaykovsky ring-closing r
FIRST ASYMMETRIC SYNTHESIS OF 4-PIPERIDONES. PREPARATION OF OPTICALLY ACTIVE DIASTEREOMERS OF 1-α-PHENYLETHYL-2-METHYL-4-PIPERIDONE
Grishina, G. V.,Potapov, V. M.,Gudasheva, T. A.,Abdulganeeva, S. A.
, p. 1132 - 1136 (2007/10/02)
The fundamental possibility of carrying out the asymmetric synthesis of 4-piperidones on the basis of the transamination of 1-substituted 2-methyl-4-piperidone methiodides by optically active α-phenylethylamine was demonstrated; the optical yield of the asymmetric transamination is 50percent.The occurrence of asymmetric synthesis was confirmed by the isolation of enantiomers of 2-methyl-4-piperidol by reduction of the individual diastereomers of 1-α-phenyl-ethyl-2-methyl-4-piperidone to the corresponding 4-piperidols with subsequent removal of the chiral substituent attached to the nitrogen atom.
