tert-butyl (R)-4-(1-hydroxyethyl)piperidine-1-carboxylate

95%

Reagent Code: #229134
label
Alias 4-[(1R)-1-hydroxyethyl]piperidine-1-carboxylic acid tert-butyl ester; (R)-1-(1-BOC-4-piperidine)ethanol
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CAS Number 1206830-71-8

science Other reagents with same CAS 1206830-71-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.31 g/mol
Formula C₁₂H₂₃NO₃
badge Registry Numbers
MDL Number MFCD22666104
inventory_2 Storage & Handling
Storage 2-8°C, Sealed

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected piperidine structure with a hydroxyethyl group makes it valuable in constructing complex molecules for central nervous system agents, including antidepressants and antipsychotics. The tert-butyl carbamate (Boc) group allows for selective protection during peptide coupling or heterocycle formation, enabling stepwise assembly in multi-step organic syntheses. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical stability and functional group compatibility.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,150.00
inventory 250mg
10-20 days ฿7,320.00
inventory 1g
10-20 days ฿19,980.00

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tert-butyl (R)-4-(1-hydroxyethyl)piperidine-1-carboxylate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected piperidine structure with a hydroxyethyl group makes it valuable in constructing complex molecules for central nervous system agents, including antidepressants and antipsychotics. The tert-butyl carbamate (Boc) group allows for selective protection during peptide coupling or heterocycle formation, enabling stepwise

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its protected piperidine structure with a hydroxyethyl group makes it valuable in constructing complex molecules for central nervous system agents, including antidepressants and antipsychotics. The tert-butyl carbamate (Boc) group allows for selective protection during peptide coupling or heterocycle formation, enabling stepwise assembly in multi-step organic syntheses. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemical stability and functional group compatibility.

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