Methyl 1-Cbz-3-methylpiperidine-3-carboxylate

≥95%

Reagent Code: #76209
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CAS Number 174543-82-9

science Other reagents with same CAS 174543-82-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.34 g/mol
Formula C₁₆H₂₁NO₄
badge Registry Numbers
MDL Number MFCD21641310
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in the preparation of pharmaceutical intermediates. It serves as a key building block in the development of various bioactive molecules, especially those targeting the central nervous system. The Cbz (carbobenzyloxy) protecting group in the structure allows for selective deprotection, enabling controlled synthesis of complex piperidine derivatives. These derivatives are often explored for their potential in drug discovery, particularly in the design of compounds with therapeutic applications such as analgesics, antipsychotics, and anticonvulsants. Additionally, its ester functionality makes it a versatile intermediate for further chemical modifications, including hydrolysis or reduction, to yield other valuable compounds.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿4,140.00
250mg
10-20 days ฿1,710.00
Methyl 1-Cbz-3-methylpiperidine-3-carboxylate
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This compound is primarily utilized in organic synthesis, particularly in the preparation of pharmaceutical intermediates. It serves as a key building block in the development of various bioactive molecules, especially those targeting the central nervous system. The Cbz (carbobenzyloxy) protecting group in the structure allows for selective deprotection, enabling controlled synthesis of complex piperidine derivatives. These derivatives are often explored for their potential in drug discovery, particularl

This compound is primarily utilized in organic synthesis, particularly in the preparation of pharmaceutical intermediates. It serves as a key building block in the development of various bioactive molecules, especially those targeting the central nervous system. The Cbz (carbobenzyloxy) protecting group in the structure allows for selective deprotection, enabling controlled synthesis of complex piperidine derivatives. These derivatives are often explored for their potential in drug discovery, particularly in the design of compounds with therapeutic applications such as analgesics, antipsychotics, and anticonvulsants. Additionally, its ester functionality makes it a versatile intermediate for further chemical modifications, including hydrolysis or reduction, to yield other valuable compounds.

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