(R)-4-Benzyl 1-Boc-2-methylpiperazine-4-carboxylate

97%

Reagent Code: #71045
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CAS Number 128102-16-9

science Other reagents with same CAS 128102-16-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 334.41 g/mol
Formula C₁₈H₂₆N₂O₄
badge Registry Numbers
MDL Number MFCD06410782
thermostat Physical Properties
Boiling Point 435.4°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

(R)-4-Benzyl 1-Boc-2-methylpiperazine-4-carboxylate is primarily used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various bioactive compounds, including potential drug candidates. Its structure is valuable for constructing piperazine-based frameworks, which are common in many therapeutic agents. This chemical is often employed in medicinal chemistry research to develop compounds targeting neurological disorders, cardiovascular diseases, and other medical conditions. Additionally, it is utilized in asymmetric synthesis to create chiral molecules, which are crucial for the development of enantiomerically pure drugs. Its protective Boc group allows for selective reactions, making it a versatile building block in multi-step synthetic processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,040.00
inventory 100mg
10-20 days ฿7,020.00

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(R)-4-Benzyl 1-Boc-2-methylpiperazine-4-carboxylate
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(R)-4-Benzyl 1-Boc-2-methylpiperazine-4-carboxylate is primarily used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of various bioactive compounds, including potential drug candidates. Its structure is valuable for constructing piperazine-based frameworks, which are common in many therapeutic agents. This chemical is often employed in medicinal chemistry research to develop compounds targeting neurological disorders, cardiovascular diseases, and other medical conditions. Additionally, it is utilized in asymmetric synthesis to create chiral molecules, which are crucial for the development of enantiomerically pure drugs. Its protective Boc group allows for selective reactions, making it a versatile building block in multi-step synthetic processes.
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