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

97%

Reagent Code: #235717
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CAS Number 1391439-19-2

science Other reagents with same CAS 1391439-19-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.68 g/mol
Formula C₁₀H₁₄ClNO₂
badge Registry Numbers
MDL Number MFCD12910779
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its enantiomerically pure structure makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in drug activity. Commonly employed in the preparation of bioactive molecules, including central nervous system agents and cardiovascular therapeutics. Also serves as a building block in medicinal chemistry for constructing complex organic molecules with high selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,930.00
inventory 100mg
10-20 days ฿9,560.00
inventory 250mg
10-20 days ฿17,470.00
(S)-Methyl 3-(1-aminoethyl)benzoate hydrochloride
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its enantiomerically pure structure makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in drug activity. Commonly employed in the preparation of bioactive molecules, including central nervous system agents and cardiovascular therapeutics. Also serves as a building block in medicinal chemistry for constructing complex organic molecules with high selectivity.

Used in the synthesis of pharmaceutical intermediates, particularly in the development of chiral drugs. Its enantiomerically pure structure makes it valuable in asymmetric synthesis, where stereochemistry plays a critical role in drug activity. Commonly employed in the preparation of bioactive molecules, including central nervous system agents and cardiovascular therapeutics. Also serves as a building block in medicinal chemistry for constructing complex organic molecules with high selectivity.

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