(R)-3-Aminomethyl-1-Boc-piperidine

98%

Reagent Code: #229929
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CAS Number 140645-23-4

science Other reagents with same CAS 140645-23-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.31 g/mol
Formula C₁₁H₂₂N₂O₂
badge Registry Numbers
MDL Number MFCD03839876
inventory_2 Storage & Handling
Density 0.997g/mLat 25℃
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of central nervous system agents, including antidepressants and antipsychotics, due to its structural compatibility with bioactive molecules. Also utilized in the creation of peptide mimetics and enzyme inhibitors, where the piperidine scaffold contributes to improved metabolic stability and receptor binding affinity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿203.50
1g
10-20 days ฿900.00
5g
10-20 days ฿3,650.00
25g
10-20 days ฿18,040.00
(R)-3-Aminomethyl-1-Boc-piperidine
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of central nervous system agents, including antidepressants and antipsychotics, due to its structural compatibility with bioactive molecules. Also utilized in the creati

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its protected amine group allows for selective reactions in multi-step organic syntheses. Commonly employed in the preparation of central nervous system agents, including antidepressants and antipsychotics, due to its structural compatibility with bioactive molecules. Also utilized in the creation of peptide mimetics and enzyme inhibitors, where the piperidine scaffold contributes to improved metabolic stability and receptor binding affinity.

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