(R)-2-(((R)-2-Hydroxy-1-phenylethyl)amino)-2-methylhexan-1-ol

95%

Reagent Code: #37434
fingerprint
CAS Number 2004679-56-3

science Other reagents with same CAS 2004679-56-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.36 g/mol
Formula C₁₅H₂₅NO₂
thermostat Physical Properties
Boiling Point 402.9±30.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.036±0.06 g/cm3(Predicted)
Storage 2-8℃

description Product Description

This compound is primarily utilized in the synthesis of chiral ligands and catalysts in asymmetric organic reactions. It plays a significant role in enantioselective transformations, such as hydrogenation and carbon-carbon bond formation, which are critical in the production of pharmaceuticals and fine chemicals. Its chiral structure allows for the creation of highly specific and efficient catalysts, enhancing the yield and purity of desired enantiomers. Additionally, it is employed in research and development for designing novel therapeutic agents, particularly in the field of medicinal chemistry, where stereochemistry is crucial for biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,600.00
inventory 25mg
10-20 days ฿4,680.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-2-(((R)-2-Hydroxy-1-phenylethyl)amino)-2-methylhexan-1-ol
No image available

This compound is primarily utilized in the synthesis of chiral ligands and catalysts in asymmetric organic reactions. It plays a significant role in enantioselective transformations, such as hydrogenation and carbon-carbon bond formation, which are critical in the production of pharmaceuticals and fine chemicals. Its chiral structure allows for the creation of highly specific and efficient catalysts, enhancing the yield and purity of desired enantiomers. Additionally, it is employed in research and devel

This compound is primarily utilized in the synthesis of chiral ligands and catalysts in asymmetric organic reactions. It plays a significant role in enantioselective transformations, such as hydrogenation and carbon-carbon bond formation, which are critical in the production of pharmaceuticals and fine chemicals. Its chiral structure allows for the creation of highly specific and efficient catalysts, enhancing the yield and purity of desired enantiomers. Additionally, it is employed in research and development for designing novel therapeutic agents, particularly in the field of medicinal chemistry, where stereochemistry is crucial for biological activity.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...