2-(2-Aminoethylthio)benzoic acid hcl

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Reagent Code: #138155
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CAS Number 14943-94-3

science Other reagents with same CAS 14943-94-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.72 g/mol
Formula C₉H₁₂ClNO₂S
badge Registry Numbers
MDL Number MFCD16661026
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

2-(2-Aminoethylthio)benzoic acid hydrochloride is a specialty chemical intermediate used in organic synthesis and medicinal chemistry. It features a benzoic acid core connected via a thioether linkage to an ethylamine chain, providing sulfur and nitrogen functional groups ideal for building complex molecules. Commonly applied as a building block in the synthesis of pharmaceutical compounds, including enzyme inhibitors, receptor ligands, and bioactive agents targeting protein interactions. Its structure supports modifications for prodrug development and studies on biomolecular binding mechanisms involving thiols and amines.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,760.00

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2-(2-Aminoethylthio)benzoic acid hcl
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2-(2-Aminoethylthio)benzoic acid hydrochloride is a specialty chemical intermediate used in organic synthesis and medicinal chemistry. It features a benzoic acid core connected via a thioether linkage to an ethylamine chain, providing sulfur and nitrogen functional groups ideal for building complex molecules. Commonly applied as a building block in the synthesis of pharmaceutical compounds, including enzyme inhibitors, receptor ligands, and bioactive agents targeting protein interactions. Its structure s

2-(2-Aminoethylthio)benzoic acid hydrochloride is a specialty chemical intermediate used in organic synthesis and medicinal chemistry. It features a benzoic acid core connected via a thioether linkage to an ethylamine chain, providing sulfur and nitrogen functional groups ideal for building complex molecules. Commonly applied as a building block in the synthesis of pharmaceutical compounds, including enzyme inhibitors, receptor ligands, and bioactive agents targeting protein interactions. Its structure supports modifications for prodrug development and studies on biomolecular binding mechanisms involving thiols and amines.

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