(S)-4-(1-((tert-Butoxycarbonyl)amino)-2-hydroxyethyl)-3-methylbenzoic acid

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Reagent Code: #232651
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CAS Number 2828028-30-2

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Weight 295.33 g/mol
Formula C₁₅H₂₁NO₅
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of beta-blockers and other cardiovascular drugs. Its hydroxyl and carboxylic acid functional groups allow for further chemical modifications, enabling the construction of complex drug molecules. The Boc-protected amine group provides stability during synthesis and can be selectively deprotected to introduce amine-containing side chains. Commonly employed in asymmetric synthesis routes where stereochemistry is critical for biological activity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿29,230.00
inventory 100mg
10-20 days ฿49,650.00
inventory 250mg
10-20 days ฿84,410.00

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(S)-4-(1-((tert-Butoxycarbonyl)amino)-2-hydroxyethyl)-3-methylbenzoic acid
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Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of beta-blockers and other cardiovascular drugs. Its hydroxyl and carboxylic acid functional groups allow for further chemical modifications, enabling the construction of complex drug molecules. The Boc-protected amine group provides stability during synthesis and can be selectively deprotected to introduce amine-containing side chains. Commonly employed in asymmetric synthesis routes where stereoc

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of beta-blockers and other cardiovascular drugs. Its hydroxyl and carboxylic acid functional groups allow for further chemical modifications, enabling the construction of complex drug molecules. The Boc-protected amine group provides stability during synthesis and can be selectively deprotected to introduce amine-containing side chains. Commonly employed in asymmetric synthesis routes where stereochemistry is critical for biological activity.

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