89451-58-1 Usage
General Description
(2S,4S)-2-Methylpiperidin-4-ol is a chemical compound that belongs to the class of piperidines. It is a stereoisomer of (2R,4S)-2-Methylpiperidin-4-ol, and the two isomers differ in the spatial arrangement of atoms. (2S,4S)-2-Methylpiperidin-4-ol is commonly used as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its specific stereochemistry makes it suitable for use in the production of certain drugs and other organic compounds. It is also used in research and development as a building block for creating new molecules with potentially beneficial properties. Additionally, (2S,4S)-2-Methylpiperidin-4-ol may have potential applications in the field of medicinal chemistry for the development of new therapeutic agents.
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 articles and documents
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. ASYMMETRIC TRANSAMINATION OF 1,1,2-TRIMETHYL-4-PIPERIDONIUM IODIDE BY (-)-α-PHENYLETHYLAMINE
Grishina, G. V.,Potapov, V. M.,Abdulganeeva, S. A.,Gudasheva, T. A.,Leshcheva, I. F.,et al.
, p. 1344 (2007/10/02)
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