(S)-2-Amino-2-(thiophen-3-yl)acetic acid

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Reagent Code: #234933
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CAS Number 1194-87-2

science Other reagents with same CAS 1194-87-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 157.19 g/mol
Formula C₆H₇NO₂S
badge Registry Numbers
MDL Number MFCD00079617
thermostat Physical Properties
Boiling Point 317.5°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of nootropic and central nervous system agents. Its structural motif is valuable in creating biologically active molecules due to the presence of both amino and carboxylic acid functional groups in a stereospecific configuration. The thiophene ring enhances binding affinity in certain receptor systems, making it useful in medicinal chemistry for designing drugs with improved selectivity and potency. Also employed in asymmetric synthesis and as an intermediate in the preparation of peptidomimetics.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,220.00
inventory 250mg
10-20 days ฿2,742.00

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(S)-2-Amino-2-(thiophen-3-yl)acetic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of nootropic and central nervous system agents. Its structural motif is valuable in creating biologically active molecules due to the presence of both amino and carboxylic acid functional groups in a stereospecific configuration. The thiophene ring enhances binding affinity in certain receptor systems, making it useful in medicinal chemistry for designing drugs with improved selectivity and potency. Also emp
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of nootropic and central nervous system agents. Its structural motif is valuable in creating biologically active molecules due to the presence of both amino and carboxylic acid functional groups in a stereospecific configuration. The thiophene ring enhances binding affinity in certain receptor systems, making it useful in medicinal chemistry for designing drugs with improved selectivity and potency. Also employed in asymmetric synthesis and as an intermediate in the preparation of peptidomimetics.
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