(R)-Methyl 4-(1-amino-2-hydroxyethyl)benzoate hydrochloride

97%

Reagent Code: #230524
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CAS Number 1196049-17-8

science Other reagents with same CAS 1196049-17-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.68 g/mol
Formula C₁₀H₁₄ClNO₃
badge Registry Numbers
MDL Number MFCD12910852
inventory_2 Storage & Handling
Storage Store in an inert gas at room temperature

description Product Description

Used in the synthesis of β-blockers, particularly in the production of chiral intermediates for pharmaceuticals. Its structure supports the development of cardioselective agents targeting hypertension and arrhythmias. The chiral center allows for selective interaction with adrenergic receptors, improving drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis routes where the hydroxy and amino functional groups are further modified to form active drug substances.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿17,160.00
250mg
10-20 days ฿34,310.00
(R)-Methyl 4-(1-amino-2-hydroxyethyl)benzoate hydrochloride
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Used in the synthesis of β-blockers, particularly in the production of chiral intermediates for pharmaceuticals. Its structure supports the development of cardioselective agents targeting hypertension and arrhythmias. The chiral center allows for selective interaction with adrenergic receptors, improving drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis routes where the hydroxy and amino functional groups are further modified to form active drug substances.

Used in the synthesis of β-blockers, particularly in the production of chiral intermediates for pharmaceuticals. Its structure supports the development of cardioselective agents targeting hypertension and arrhythmias. The chiral center allows for selective interaction with adrenergic receptors, improving drug efficacy and reducing side effects. Commonly employed in asymmetric synthesis routes where the hydroxy and amino functional groups are further modified to form active drug substances.

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