(R)-2-Amino-3-(4-vinylphenyl)propanoic acid hydrochloride

98%

Reagent Code: #229403
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CAS Number 2682097-68-1

science Other reagents with same CAS 2682097-68-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.69 g/mol
Formula C₁₁H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD32874272
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of neuroactive compounds and enzyme inhibitors. Its vinyl-substituted aromatic group allows for further functionalization via cross-coupling reactions or polymerization, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in asymmetric synthesis due to the presence of a stereogenic center, enabling the preparation of enantiomerically pure drugs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,710.00
inventory 250mg
10-20 days ฿32,490.00

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(R)-2-Amino-3-(4-vinylphenyl)propanoic acid hydrochloride
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of neuroactive compounds and enzyme inhibitors. Its vinyl-substituted aromatic group allows for further functionalization via cross-coupling reactions or polymerization, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in asymmetric synthesis due to the presence of a stereogenic center, enabling the preparation of enantiomerically pure drugs

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of neuroactive compounds and enzyme inhibitors. Its vinyl-substituted aromatic group allows for further functionalization via cross-coupling reactions or polymerization, making it valuable in medicinal chemistry for structure-activity relationship studies. Also employed in asymmetric synthesis due to the presence of a stereogenic center, enabling the preparation of enantiomerically pure drugs.

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