(S)-tert-Butyl 1-methyl-2-oxoimidazolidine-4-carboxylate

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Reagent Code: #234950
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CAS Number 83056-79-5

science Other reagents with same CAS 83056-79-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.24 g/mol
Formula C₉H₁₆N₂O₃
badge Registry Numbers
MDL Number MFCD09952527
thermostat Physical Properties
Boiling Point 347.4°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its imidazolidinone structure supports the formation of peptidomimetics and other heterocyclic compounds, making it valuable in medicinal chemistry for drug design. Commonly employed in asymmetric synthesis to introduce stereochemical control, especially in the preparation of biologically active molecules such as protease inhibitors or central nervous system agents. The tert-butyl ester protection allows for selective deprotection and further functionalization in multi-step synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿174.00
inventory 1g
10-20 days ฿310.00
inventory 5g
10-20 days ฿1,530.00
inventory 25g
10-20 days ฿5,750.00
(S)-tert-Butyl 1-methyl-2-oxoimidazolidine-4-carboxylate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its imidazolidinone structure supports the formation of peptidomimetics and other heterocyclic compounds, making it valuable in medicinal chemistry for drug design. Commonly employed in asymmetric synthesis to introduce stereochemical control, especially in the preparation of biologically active molecules such as protease inhi

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its imidazolidinone structure supports the formation of peptidomimetics and other heterocyclic compounds, making it valuable in medicinal chemistry for drug design. Commonly employed in asymmetric synthesis to introduce stereochemical control, especially in the preparation of biologically active molecules such as protease inhibitors or central nervous system agents. The tert-butyl ester protection allows for selective deprotection and further functionalization in multi-step synthetic routes.

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