(R)-()-4-Methoxy-α-methylbenzylamine

98%

Reagent Code: #71670
label
Alias (R)-(+)-1-(4-methoxyphenyl)ethylamine; (R)-(+)-1-(4-methoxyphenyl)ethylamine, (R)-p-methoxy phenylethylamine, (R)-(+)-4-methoxy-α-methylbenzylamine
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CAS Number 22038-86-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.21 g/mol
Formula C₉H₁₃NO
badge Registry Numbers
MDL Number MFCD00671659
thermostat Physical Properties
Boiling Point 65°C 0,4mm
inventory_2 Storage & Handling
Density 1.024 g/mL at 20 °C(lit.)
Storage room temperature, sealed

description Product Description

(R)-()-4-Methoxy-α-methylbenzylamine is primarily used as a chiral building block in the synthesis of various pharmaceuticals. Its chiral nature makes it valuable in the production of enantiomerically pure compounds, which are crucial for drugs that require specific stereochemistry to achieve desired biological activity. This compound is often employed in asymmetric synthesis, where it serves as a chiral auxiliary or ligand to induce stereoselectivity in chemical reactions. Additionally, it finds application in the development of agrochemicals and fine chemicals, where its structural framework contributes to the creation of biologically active molecules with enhanced efficacy and selectivity.

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Test Parameter Specification
Purity (GC) 98-100%
Selective Chiral HPLC 98-100
Specific Rotation (α20/D neat) 30-34

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿9,580.00
inventory 1g
10-20 days ฿590.00
inventory 5g
10-20 days ฿1,990.00
(R)-()-4-Methoxy-α-methylbenzylamine
(R)-()-4-Methoxy-α-methylbenzylamine is primarily used as a chiral building block in the synthesis of various pharmaceuticals. Its chiral nature makes it valuable in the production of enantiomerically pure compounds, which are crucial for drugs that require specific stereochemistry to achieve desired biological activity. This compound is often employed in asymmetric synthesis, where it serves as a chiral auxiliary or ligand to induce stereoselectivity in chemical reactions. Additionally, it finds application in the development of agrochemicals and fine chemicals, where its structural framework contributes to the creation of biologically active molecules with enhanced efficacy and selectivity.
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