1174386-89-0 | 1-Piperidinecarboxylic acid, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-(hydroxymethyl)-, 1,1-dimethylethyl ester, (2r,3s)-

Packsize	Purity	Availability	Price	Discounted Price
100mg	95%	in stock	$341.00	$239.00
250mg	95%	in stock	$545.00	$382.00
500mg	95%	in stock	$907.00	$635.00

Description

• Catalog Number: AI66983
• Chemical Name: 1-Piperidinecarboxylic acid, 3-[[(1,1-dimethylethyl)dimethylsilyl]oxy]-2-(hydroxymethyl)-, 1,1-dimethylethyl ester, (2r,3s)-
• CAS Number: 1174386-89-0
• Molecular Formula: C17H35NO4Si
• Molecular Weight: 345.5496
• MDL Number: MFCD29472371
• SMILES: OC[C@@H]1[C@H](CCCN1C(=O)OC(C)(C)C)O[Si](C(C)(C)C)(C)C

Upstream Synthesis Route

The compound (2R,3S)-tert-Butyl 3-((tert-butyldimethylsilyl)oxy)-2-(hydroxymethyl)piperidine-1-carboxylate is commonly utilized in chemical synthesis as a versatile building block due to its unique structure and reactivity. This compound serves as a valuable intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals.One important application of (2R,3S)-tert-Butyl 3-((tert-butyldimethylsilyl)oxy)-2-(hydroxymethyl)piperidine-1-carboxylate is as a chiral auxiliary in asymmetric synthesis. Its chiral nature allows for the creation of enantiomerically pure compounds, which is crucial in drug discovery and development. By utilizing this compound in synthesis, chemists can efficiently access a wide variety of chiral molecules with high selectivity and precision.Furthermore, the tert-butyldimethylsilyl protecting group on the piperidine ring provides stability and control during various chemical reactions, making it a valuable tool in synthetic organic chemistry. Overall, (2R,3S)-tert-Butyl 3-((tert-butyldimethylsilyl)oxy)-2-(hydroxymethyl)piperidine-1-carboxylate plays a significant role in the construction of complex molecules and the development of novel bioactive compounds.