(3R,4S)-tert-Butyl 3,4-dihydroxypyrrolidine-1-carboxylate

97%

Reagent Code: #230173
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CAS Number 186393-22-6

science Other reagents with same CAS 186393-22-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.24 g/mol
Formula C₉H₁₇NO₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of antidiabetic drugs such as DPP-4 inhibitors. Its stereochemistry allows for selective interactions in biological systems, enhancing drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis to introduce specific functional groups with high enantiomeric purity. Also utilized in the development of protease inhibitors and other bioactive molecules requiring precise 3D structural control.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿640.00
100mg
10-20 days ฿1,450.00
250mg
10-20 days ฿2,890.00
1g
10-20 days ฿9,840.00
5g
10-20 days ฿34,020.00
(3R,4S)-tert-Butyl 3,4-dihydroxypyrrolidine-1-carboxylate
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of antidiabetic drugs such as DPP-4 inhibitors. Its stereochemistry allows for selective interactions in biological systems, enhancing drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis to introduce specific functional groups with high enantiomeric purity. Also utilized in the development of protease inhibitors and other bioactive molecules requiring precise 3D structural

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of antidiabetic drugs such as DPP-4 inhibitors. Its stereochemistry allows for selective interactions in biological systems, enhancing drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis to introduce specific functional groups with high enantiomeric purity. Also utilized in the development of protease inhibitors and other bioactive molecules requiring precise 3D structural control.

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