trans-tert-Butyl 3-cyano-4-hydroxypyrrolidine-1-carboxylate

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Reagent Code: #140920
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CAS Number 215922-85-3

science Other reagents with same CAS 215922-85-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.25 g/mol
Formula C₁₀H₁₆N₂O₃
badge Registry Numbers
MDL Number MFCD09608027
thermostat Physical Properties
Boiling Point 361.4±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.19±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antidiabetic drugs. Its structure supports the formation of pyrrolidine-based inhibitors that target enzymes involved in glucose metabolism. The cyano and hydroxyl functional groups allow for further chemical modifications, enabling the creation of more complex bioactive molecules. Commonly employed in medicinal chemistry for building chiral scaffolds due to its stereochemical stability and reactivity profile.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,500.00

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trans-tert-Butyl 3-cyano-4-hydroxypyrrolidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antidiabetic drugs. Its structure supports the formation of pyrrolidine-based inhibitors that target enzymes involved in glucose metabolism. The cyano and hydroxyl functional groups allow for further chemical modifications, enabling the creation of more complex bioactive molecules. Commonly employed in medicinal chemistry for building chiral scaffolds due to its stereochemical stability and reactivity

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of antidiabetic drugs. Its structure supports the formation of pyrrolidine-based inhibitors that target enzymes involved in glucose metabolism. The cyano and hydroxyl functional groups allow for further chemical modifications, enabling the creation of more complex bioactive molecules. Commonly employed in medicinal chemistry for building chiral scaffolds due to its stereochemical stability and reactivity profile.

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