(R)-tert-Butyl 2-methylpyrrolidine-1-carboxylate

98%

Reagent Code: #232285
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CAS Number 157007-54-0

science Other reagents with same CAS 157007-54-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 185.26 g/mol
Formula C₁₀H₁₉NO₂
badge Registry Numbers
MDL Number MFCD09261335
thermostat Physical Properties
Boiling Point 234.0 ± 9.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its protected amine group and chiral center make it valuable in asymmetric synthesis, enabling the construction of complex molecules with high enantiomeric purity. Commonly employed in medicinal chemistry for drug discovery programs, especially in the preparation of centrally acting agents and enzyme inhibitors. The compound is also utilized in the preparation of catalysts and ligands for enantioselective transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,890.00
inventory 250mg
10-20 days ฿3,220.00
inventory 1g
10-20 days ฿10,610.00
(R)-tert-Butyl 2-methylpyrrolidine-1-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) where stereochemistry plays a critical role in biological activity. Its protected amine group and chiral center make it valuable in asymmetric synthesis, enabling the construction of complex molecules with high enantiomeric purity. Commonly employed in medicinal chemistry for drug discovery programs, especially in the preparation of centrally acting agents and e

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its protected amine group and chiral center make it valuable in asymmetric synthesis, enabling the construction of complex molecules with high enantiomeric purity. Commonly employed in medicinal chemistry for drug discovery programs, especially in the preparation of centrally acting agents and enzyme inhibitors. The compound is also utilized in the preparation of catalysts and ligands for enantioselective transformations.

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