(R)-tert-butyl 3-methyl-5-oxopiperidine-1-carboxylate

95%

Reagent Code: #230889
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CAS Number 1601475-90-4

science Other reagents with same CAS 1601475-90-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.2739 g/mol
Formula C₁₁H₁₉NO₃
badge Registry Numbers
MDL Number MFCD30207802
inventory_2 Storage & Handling
Storage 2-8°C, inert atmosphere

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure supports the construction of complex nitrogen-containing heterocycles, making it valuable in medicinal chemistry for drug discovery. Commonly employed in asymmetric synthesis to introduce stereocenters in target molecules, especially in the preparation of enzyme inhibitors and central nervous system agents. The tert-butyl carbamate (Boc) group allows for selective protection of amines, enabling controlled stepwise reactions in multi-step synthetic routes.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿16,700.00
250mg
10-20 days ฿33,960.00
1g
10-20 days ฿48,640.00
(R)-tert-butyl 3-methyl-5-oxopiperidine-1-carboxylate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure supports the construction of complex nitrogen-containing heterocycles, making it valuable in medicinal chemistry for drug discovery. Commonly employed in asymmetric synthesis to introduce stereocenters in target molecules, especially in the preparation of enzyme inhibitors and central nervous system agents. The tert-

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure supports the construction of complex nitrogen-containing heterocycles, making it valuable in medicinal chemistry for drug discovery. Commonly employed in asymmetric synthesis to introduce stereocenters in target molecules, especially in the preparation of enzyme inhibitors and central nervous system agents. The tert-butyl carbamate (Boc) group allows for selective protection of amines, enabling controlled stepwise reactions in multi-step synthetic routes.

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