(R)-2-((5-Chloro-4-iodopyridin-2-yl)amino)propan-1-ol

≥95%

Reagent Code: #113505
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CAS Number 1799412-23-9

science Other reagents with same CAS 1799412-23-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 312.54 g/mol
Formula C₈H₁₀ClIN₂O
badge Registry Numbers
MDL Number MFCD25459280
thermostat Physical Properties
Boiling Point 427.7°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting specific enzyme systems or receptors. Its structure is often exploited in the development of potential drug candidates, especially in the design of molecules with therapeutic applications for neurological disorders or other conditions influenced by the modulation of specific biochemical pathways. Researchers also explore its use in creating chiral compounds, leveraging its stereochemistry to enhance the selectivity and efficacy of drug molecules. Additionally, it may be employed in studies investigating the structure-activity relationship (SAR) of related compounds to optimize their pharmacological properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,692.00
inventory 100mg
10-20 days ฿1,125.00
inventory 1g
10-20 days ฿4,221.00

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(R)-2-((5-Chloro-4-iodopyridin-2-yl)amino)propan-1-ol
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This chemical is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting specific enzyme systems or receptors. Its structure is often exploited in the development of potential drug candidates, especially in the design of molecules with therapeutic applications for neurological disorders or other conditions influenced by the modulation of specific biochemical pathways. Researchers also explore its use in creating chiral compounds, leveraging its stereochemistry to enhance the selectivity and efficacy of drug molecules. Additionally, it may be employed in studies investigating the structure-activity relationship (SAR) of related compounds to optimize their pharmacological properties.
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