S-1-Boc-3-(hydroxymethyl)piperidine

98%

Reagent Code: #234232
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Alias (S)-1-Boc-3-hydroxymethylpiperidine
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CAS Number 140695-84-7

science Other reagents with same CAS 140695-84-7

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Weight 215.29 g/mol
Formula C₁₁H₂₁NO₃
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MDL Number MFCD02683203
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring piperidine scaffolds. Its protected amine and hydroxymethyl functional groups allow selective reactions, making it valuable in constructing complex molecules for central nervous system drugs, including antidepressants and antipsychotics. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemistry and functional group compatibility in multi-step syntheses.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿168.00
inventory 5g
10-20 days ฿1,020.00
inventory 25g
10-20 days ฿4,940.00

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S-1-Boc-3-(hydroxymethyl)piperidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring piperidine scaffolds. Its protected amine and hydroxymethyl functional groups allow selective reactions, making it valuable in constructing complex molecules for central nervous system drugs, including antidepressants and antipsychotics. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemistry and

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring piperidine scaffolds. Its protected amine and hydroxymethyl functional groups allow selective reactions, making it valuable in constructing complex molecules for central nervous system drugs, including antidepressants and antipsychotics. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its stereochemistry and functional group compatibility in multi-step syntheses.

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