(S)-tert-Butyl (3-oxocyclopentyl)carbamate

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Reagent Code: #235633
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CAS Number 167298-40-0

science Other reagents with same CAS 167298-40-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.25 g/mol
Formula C₁₀H₁₇NO₃
badge Registry Numbers
MDL Number MFCD18089809
thermostat Physical Properties
Boiling Point 319.2±31.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where chirality plays a critical role. Its structure contains both a protected amine and a ketone functional group, making it valuable in multi-step organic syntheses. The tert-butyl carbamate group serves as a protecting group for the amine, allowing selective reactions at other sites, while the ketone can undergo transformations such as reductions, Grignard additions, or reductive aminations. Commonly employed in the preparation of cyclopentane-based scaffolds found in medicinal chemistry, especially in the discovery of enzyme inhibitors and central nervous system agents. Its chiral center allows for stereoselective synthesis, enhancing the efficacy and specificity of the final drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,750.00
inventory 250mg
10-20 days ฿3,330.00
inventory 500mg
10-20 days ฿6,630.00
inventory 1g
10-20 days ฿12,210.00
inventory 5g
10-20 days ฿40,080.00
(S)-tert-Butyl (3-oxocyclopentyl)carbamate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where chirality plays a critical role. Its structure contains both a protected amine and a ketone functional group, making it valuable in multi-step organic syntheses. The tert-butyl carbamate group serves as a protecting group for the amine, allowing selective reactions at other sites, while the ketone can undergo transformations such as reductions, Grignard additions, or redu

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where chirality plays a critical role. Its structure contains both a protected amine and a ketone functional group, making it valuable in multi-step organic syntheses. The tert-butyl carbamate group serves as a protecting group for the amine, allowing selective reactions at other sites, while the ketone can undergo transformations such as reductions, Grignard additions, or reductive aminations. Commonly employed in the preparation of cyclopentane-based scaffolds found in medicinal chemistry, especially in the discovery of enzyme inhibitors and central nervous system agents. Its chiral center allows for stereoselective synthesis, enhancing the efficacy and specificity of the final drug candidates.

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