(3R,4R)-rel-tert-Butyl 4-(aminomethyl)-3-hydroxypiperidine-1-carboxylate

97%

Reagent Code: #229299
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CAS Number 219975-84-5

science Other reagents with same CAS 219975-84-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.3 g/mol
Formula C₁₁H₂₂N₂O₃
badge Registry Numbers
MDL Number MFCD18381924
thermostat Physical Properties
Melting Point 178 °C
Boiling Point 346.2±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.115±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used in pharmaceutical synthesis as a chiral building block for active pharmaceutical ingredients (APIs), particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of potent and selective receptor modulators due to the presence of functional groups in defined stereochemistry. Commonly employed in the preparation of neurologically active compounds, including those targeting pain, depression, and neurological disorders. The protected amine and hydroxyl groups allow for selective modifications during multi-step synthesis, making it valuable in medicinal chemistry for optimizing drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,310.00
250mg
10-20 days ฿7,200.00
1g
10-20 days ฿15,780.00
5g
10-20 days ฿48,820.00
(3R,4R)-rel-tert-Butyl 4-(aminomethyl)-3-hydroxypiperidine-1-carboxylate
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Used in pharmaceutical synthesis as a chiral building block for active pharmaceutical ingredients (APIs), particularly in the development of central nervous system (CNS) agents. Its structure supports the creation of potent and selective receptor modulators due to the presence of functional groups in defined stereochemistry. Commonly employed in the preparation of neurologically active compounds, including those targeting pain, depression, and neurological disorders. The protected amine and hydroxyl groups allow for selective modifications during multi-step synthesis, making it valuable in medicinal chemistry for optimizing drug candidates.
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