rel-1-((1R,2R)-2-(Dimethylamino)cyclohexyl)-3-phenylthiourea

95%

Reagent Code: #229260
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CAS Number 1398733-83-9

science Other reagents with same CAS 1398733-83-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 277.43 g/mol
Formula C₁₅H₂₃N₃S
thermostat Physical Properties
Boiling Point 388.3±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.12±0.1 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of centrally acting muscle relaxants. It exhibits activity as an adrenergic agent, influencing alpha-2 receptors, which contributes to its muscle relaxant and analgesic properties. Commonly employed in research settings for studying receptor selectivity and structure-activity relationships in cyclohexyl-based amines. Also utilized in the preparation of chiral ligands for asymmetric synthesis due to its stereochemical configuration.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,720.00
inventory 250mg
10-20 days ฿14,810.00
inventory 1g
10-20 days ฿39,990.00

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rel-1-((1R,2R)-2-(Dimethylamino)cyclohexyl)-3-phenylthiourea
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of centrally acting muscle relaxants. It exhibits activity as an adrenergic agent, influencing alpha-2 receptors, which contributes to its muscle relaxant and analgesic properties. Commonly employed in research settings for studying receptor selectivity and structure-activity relationships in cyclohexyl-based amines. Also utilized in the preparation of chiral ligands for asymmetric synthesis due to its s

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of centrally acting muscle relaxants. It exhibits activity as an adrenergic agent, influencing alpha-2 receptors, which contributes to its muscle relaxant and analgesic properties. Commonly employed in research settings for studying receptor selectivity and structure-activity relationships in cyclohexyl-based amines. Also utilized in the preparation of chiral ligands for asymmetric synthesis due to its stereochemical configuration.

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