
CAS 180854-44-8
:(2S)-N-tert-butoxycarbonyl-4-oxopiperidine-2-carboxylic acid ethyl ester
Description:
(2S)-N-tert-butoxycarbonyl-4-oxopiperidine-2-carboxylic acid ethyl ester, with CAS number 180854-44-8, is a chemical compound that belongs to the class of piperidine derivatives. It features a piperidine ring substituted with a tert-butoxycarbonyl (Boc) group, which is commonly used in organic synthesis for protecting amines. The compound also contains a carboxylic acid moiety, which is esterified with an ethyl group, enhancing its solubility and reactivity. This compound is characterized by its chiral center at the 2-position of the piperidine ring, contributing to its stereochemical properties. It is typically utilized in the synthesis of various pharmaceuticals and bioactive molecules due to its functional groups that allow for further chemical modifications. The presence of the oxo group at the 4-position adds to its reactivity, making it a valuable intermediate in organic synthesis. Overall, this compound is significant in medicinal chemistry and synthetic organic chemistry for its versatility and functional characteristics.
Formula:C10H17NO3
Synonyms:- Ethyl (S)-1-Boc-4-Oxopiperidine-2-Carboxylate
- 1,2-Piperidinedicarboxylic acid, 4-oxo-, 1-(1,1-diMethylethyl) 2-ethyl ester, (2S)-
- (S)-1-Boc-4-oxo-piperidine-2-carboxylic acid methyl este
- (S)-1-Boc-4-Oxo-Piperidine-2-Carboxylic Acid Methyl Ester
- Ethyl (S)-N-(tert-butoxycarbonyl)-4-oxo-2-pipecolate
- Pbn20120647
- (S)-1-Boc-4-oxo-piperidine-2-carboxylic acid methyl ester ee
- Ethyl (S)-(-)-1-Boc-4-oxopiperidine-2-carboxylate, 95%
- 1-O-tert-butyl 2-O-ethyl (2S)-4-oxopiperidine-1,2-dicarboxylate
- 1-tert-butyl 2-ethyl (2S)-4-oxopiperidine-1,2-dicarboxylate
- (S)-1-Boc-4-oxo-piperidine-2-carboxylic acid ethyl ester
- (S)-1-Boc-4-oxo-piperidin...
- (S)-1-tert-Butyl 2-ethyl 4-oxopiperidine-1,2-dicarboxylate
- See more synonyms
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Found 4 products.
Ethyl (S)-(-)-1-Boc-4-oxopiperidine-2-carboxylate, 95%
CAS:<p>1-Boc-4-oxopiperidine-2-carboxylate participates in the one-pot in situ formation and reaction of trimethyl (trichloromethyl) silane which finds application in the synthesis of 2, 2, 2-trichloromethylcarbinols. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar prod</p>Formula:C13H21NO5Purity:95%Color and Shape:Pale yellow, Liquid.Molecular weight:271.31Ethyl (s)-1-boc-4-oxopiperidine-2-carboxylate
CAS:Formula:C13H21NO5Purity:97%Color and Shape:LiquidMolecular weight:271.3095Ethyl (S)-1-Boc-4-oxopiperidine-2-carboxylate
CAS:<p>Ethyl (S)-1-Boc-4-oxopiperidine-2-carboxylate</p>Purity:95%Molecular weight:271.31g/mol(S)-1-tert-Butyl 2-ethyl 4-oxopiperidine-1,2-dicarboxylate
CAS:Formula:C13H21NO5Purity:97%Molecular weight:271.313



