Trans-4-(Dimethylamino)Cyclohexanol

≥98%

Reagent Code: #241089
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CAS Number 103023-51-4

science Other reagents with same CAS 103023-51-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.23 g/mol
Formula C₈H₁₇NO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the development of pharmaceuticals, particularly in the creation of analgesic and anti-inflammatory agents. Its structure allows for effective modulation of biological activity in drug candidates, making it valuable in medicinal chemistry research. It is also employed in the synthesis of specialty amines used in asymmetric catalysis and chiral ligand systems. Due to its functional group arrangement, it serves as a building block for nitrogen-containing heterocycles and is utilized in the optimization of drug solubility and bioavailability.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,610.00
Trans-4-(Dimethylamino)Cyclohexanol
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Used primarily as an intermediate in organic synthesis, this compound plays a key role in the development of pharmaceuticals, particularly in the creation of analgesic and anti-inflammatory agents. Its structure allows for effective modulation of biological activity in drug candidates, making it valuable in medicinal chemistry research. It is also employed in the synthesis of specialty amines used in asymmetric catalysis and chiral ligand systems. Due to its functional group arrangement, it serves as a b

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the development of pharmaceuticals, particularly in the creation of analgesic and anti-inflammatory agents. Its structure allows for effective modulation of biological activity in drug candidates, making it valuable in medicinal chemistry research. It is also employed in the synthesis of specialty amines used in asymmetric catalysis and chiral ligand systems. Due to its functional group arrangement, it serves as a building block for nitrogen-containing heterocycles and is utilized in the optimization of drug solubility and bioavailability.

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