(S)-Methyl 2-amino-3-(thiophen-2-yl)propanoate hydrochloride

95%

Reagent Code: #233189
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CAS Number 137490-86-9

science Other reagents with same CAS 137490-86-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.7 g/mol
Formula C₈H₁₂ClNO₂S
badge Registry Numbers
MDL Number MFCD24434989
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors and antiviral agents. Its structure supports the development of biologically active molecules with high enantioselectivity. Commonly employed in the preparation of thrombin inhibitors and other enzyme-targeted drugs due to the stability and reactivity of the thiophene ring combined with the amino ester functionality. Widely utilized in medicinal chemistry for structure-activity relationship (SAR) studies and in the development of peptidomimetic compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,990.00
inventory 1g
10-20 days ฿10,690.00
(S)-Methyl 2-amino-3-(thiophen-2-yl)propanoate hydrochloride
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Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors and antiviral agents. Its structure supports the development of biologically active molecules with high enantioselectivity. Commonly employed in the preparation of thrombin inhibitors and other enzyme-targeted drugs due to the stability and reactivity of the thiophene ring combined with the amino ester functionality. Widely utilized in medicinal chemistry for structure-activity rel

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors and antiviral agents. Its structure supports the development of biologically active molecules with high enantioselectivity. Commonly employed in the preparation of thrombin inhibitors and other enzyme-targeted drugs due to the stability and reactivity of the thiophene ring combined with the amino ester functionality. Widely utilized in medicinal chemistry for structure-activity relationship (SAR) studies and in the development of peptidomimetic compounds.

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