(S)-1-(2-Chloropyrimidin-4-yl)pyrrolidin-3-ol

95%

Reagent Code: #233238
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CAS Number 1379439-07-2

science Other reagents with same CAS 1379439-07-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.64 g/mol
Formula C₈H₁₀ClN₃O
badge Registry Numbers
MDL Number MFCD18380430
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors. Its structural features enable selective binding to enzyme targets, making it valuable in the production of active pharmaceutical ingredients for oncology and inflammatory disease treatments. The stereochemistry at the pyrrolidinol center enhances biological activity and selectivity, which is critical for drug efficacy and safety. Commonly employed in late-stage functionalization processes to build complex drug molecules with high enantiomeric purity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,060.00
inventory 250mg
10-20 days ฿22,180.00
(S)-1-(2-Chloropyrimidin-4-yl)pyrrolidin-3-ol
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors. Its structural features enable selective binding to enzyme targets, making it valuable in the production of active pharmaceutical ingredients for oncology and inflammatory disease treatments. The stereochemistry at the pyrrolidinol center enhances biological activity and selectivity, which is critical for drug efficacy and safety. Commonly employed in late-stage functionaliza

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors. Its structural features enable selective binding to enzyme targets, making it valuable in the production of active pharmaceutical ingredients for oncology and inflammatory disease treatments. The stereochemistry at the pyrrolidinol center enhances biological activity and selectivity, which is critical for drug efficacy and safety. Commonly employed in late-stage functionalization processes to build complex drug molecules with high enantiomeric purity.

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