(R)-Methyl 3-(1-aminoethyl)benzoate hydrochloride

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Reagent Code: #113546
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CAS Number 1236353-78-8

science Other reagents with same CAS 1236353-78-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.68 g/mol
Formula C₁₀H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD12910778
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with specific stereochemistry. It plays a role in the production of enantiomerically pure compounds, which are critical for drugs targeting neurological and cardiovascular disorders. Its hydrochloride form enhances stability and solubility, making it suitable for use in various organic reactions and drug formulation processes. Additionally, it is employed in research for studying chiral catalysts and asymmetric synthesis methods.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿34,947.00
inventory 100mg
10-20 days ฿8,802.00
inventory 250mg
10-20 days ฿13,977.00

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(R)-Methyl 3-(1-aminoethyl)benzoate hydrochloride
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with specific stereochemistry. It plays a role in the production of enantiomerically pure compounds, which are critical for drugs targeting neurological and cardiovascular disorders. Its hydrochloride form enhances stability and solubility, making it suitable for use in various organic reactions and drug formulation processes. Additionally, it is employed in resear
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) with specific stereochemistry. It plays a role in the production of enantiomerically pure compounds, which are critical for drugs targeting neurological and cardiovascular disorders. Its hydrochloride form enhances stability and solubility, making it suitable for use in various organic reactions and drug formulation processes. Additionally, it is employed in research for studying chiral catalysts and asymmetric synthesis methods.
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