(S)-Methyl 4-(1-aminoethyl)benzoate

98%

Reagent Code: #234919
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CAS Number 222714-37-6

science Other reagents with same CAS 222714-37-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.22 g/mol
Formula C₁₀H₁₃NO₂
thermostat Physical Properties
Boiling Point 281.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its enantiomerically pure structure makes it valuable for creating active pharmaceutical ingredients with high stereoselectivity. Commonly employed in asymmetric synthesis routes where the (S)-configuration is required for biological activity. Also utilized in the development of optically active esters and amines through selective transformations of the amino and ester functional groups.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿350.00
inventory 1g
10-20 days ฿750.00
inventory 5g
10-20 days ฿3,740.00
(S)-Methyl 4-(1-aminoethyl)benzoate
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its enantiomerically pure structure makes it valuable for creating active pharmaceutical ingredients with high stereoselectivity. Commonly employed in asymmetric synthesis routes where the (S)-configuration is required for biological activity. Also utilized in the development of optically active esters and amines through selective transformations of the amino

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. Its enantiomerically pure structure makes it valuable for creating active pharmaceutical ingredients with high stereoselectivity. Commonly employed in asymmetric synthesis routes where the (S)-configuration is required for biological activity. Also utilized in the development of optically active esters and amines through selective transformations of the amino and ester functional groups.

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