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

95%

Reagent Code: #228750
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CAS Number 1083089-94-4

science Other reagents with same CAS 1083089-94-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.64 g/mol
Formula C₈H₁₀ClN₃O
badge Registry Numbers
MDL Number MFCD18380429
thermostat Physical Properties
Boiling Point 416.3±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.432±0.06 g/cm3(Predicted)
Storage 2-8°C, 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 drugs for oncology and inflammatory diseases. The compound's stereochemistry enhances biological activity and specificity, which is critical for optimizing drug efficacy and reducing off-target effects. It is commonly employed in late-stage functionalization processes during API manufacturing.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,800.00
inventory 250mg
10-20 days ฿18,350.00
inventory 1g
10-20 days ฿49,510.00
(R)-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 drugs for oncology and inflammatory diseases. The compound's stereochemistry enhances biological activity and specificity, which is critical for optimizing drug efficacy and reducing off-target effects. It is commonly employed in late-stage functionalization processes d

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 drugs for oncology and inflammatory diseases. The compound's stereochemistry enhances biological activity and specificity, which is critical for optimizing drug efficacy and reducing off-target effects. It is commonly employed in late-stage functionalization processes during API manufacturing.

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