(R)-tert-Butyl 3-(methoxymethyl)piperazine-1-carboxylate

≥95%

Reagent Code: #113553
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CAS Number 1359658-32-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.30 g/mol
Formula C₁₁H₂₂N₂O₃
badge Registry Numbers
MDL Number MFCD19688482
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a piperazine ring, makes it a valuable building block for developing drugs targeting neurological and psychiatric disorders. The presence of the tert-butyl group and methoxymethyl moiety enhances its stability and reactivity, allowing for precise modifications during drug development. It is often employed in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) agents. Additionally, its chiral nature enables the creation of enantiomerically pure compounds, which are critical for optimizing drug efficacy and reducing side effects.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿36,300.00
inventory 250mg
10-20 days ฿14,360.00
inventory 100mg
10-20 days ฿8,860.00
(R)-tert-Butyl 3-(methoxymethyl)piperazine-1-carboxylate
This compound is primarily utilized in the pharmaceutical industry as an intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its structure, featuring a piperazine ring, makes it a valuable building block for developing drugs targeting neurological and psychiatric disorders. The presence of the tert-butyl group and methoxymethyl moiety enhances its stability and reactivity, allowing for precise modifications during drug development. It is often employed in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) agents. Additionally, its chiral nature enables the creation of enantiomerically pure compounds, which are critical for optimizing drug efficacy and reducing side effects.
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