(S)-(-)-N-Benzyl-α-methylbenzylamine

97%

Reagent Code: #71665
label
Alias (S)-(-)-N-Benzyl-1-phenyl-ethylamine
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CAS Number 17480-69-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.3 g/mol
Formula C₆H₅CHCH₃NHCH₂C₆H₅
badge Registry Numbers
MDL Number MFCD00066325
thermostat Physical Properties
Boiling Point 171 °C15 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.01 g/mL at 25 °C(lit.)
Storage room temperature

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. It is employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where stereoselectivity is crucial. The compound is also utilized in the resolution of racemic mixtures, helping to separate enantiomers for specific applications. Additionally, it serves as a building block in the development of chiral ligands for catalytic processes, enhancing the efficiency and selectivity of chemical reactions.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance Colorless to light yellow to brown clear liquid
Purity 96.5-100
Specific rotation [α]20D -38.0 to -41.0 deg (neat)
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿320.00
inventory 25g
10-20 days ฿1,150.00
inventory 5g
10-20 days ฿390.00
inventory 100g
10-20 days ฿3,800.00
(S)-(-)-N-Benzyl-α-methylbenzylamine
Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure compounds. It is employed in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals where stereoselectivity is crucial. The compound is also utilized in the resolution of racemic mixtures, helping to separate enantiomers for specific applications. Additionally, it serves as a building block in the development of chiral ligands for catalytic processes, enhancing the efficiency and selectivity of chemical reactions.
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