(R)-1-tert-Butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate

98%

Reagent Code: #230511
fingerprint
CAS Number 1799811-83-8

science Other reagents with same CAS 1799811-83-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.28 g/mol
Formula C₁₂H₁₉NO₅
badge Registry Numbers
MDL Number MFCD12547038
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring stereochemical control. Its protected piperidine structure with a ketone functionality allows for selective transformations, making it valuable in constructing complex nitrogen-containing heterocycles. Commonly employed in medicinal chemistry for the preparation of protease inhibitors and central nervous system agents. The tert-butyl and methyl ester groups facilitate stepwise deprotection and coupling reactions, enabling efficient route design in multi-step syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,220.00
inventory 1g
10-20 days ฿3,670.00
inventory 5g
10-20 days ฿15,010.00
inventory 25g
10-20 days ฿75,030.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-1-tert-Butyl 2-methyl 4-oxopiperidine-1,2-dicarboxylate
No image available

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring stereochemical control. Its protected piperidine structure with a ketone functionality allows for selective transformations, making it valuable in constructing complex nitrogen-containing heterocycles. Commonly employed in medicinal chemistry for the preparation of protease inhibitors and central nervous system agents. The tert-butyl and methyl ester groups facilitate stepwi

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules requiring stereochemical control. Its protected piperidine structure with a ketone functionality allows for selective transformations, making it valuable in constructing complex nitrogen-containing heterocycles. Commonly employed in medicinal chemistry for the preparation of protease inhibitors and central nervous system agents. The tert-butyl and methyl ester groups facilitate stepwise deprotection and coupling reactions, enabling efficient route design in multi-step syntheses.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...