S-Benzyl 2-aminoethanethioate

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Reagent Code: #124057
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CAS Number 754172-97-9

science Other reagents with same CAS 754172-97-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.25 g/mol
Formula C₉H₁₁NOS
badge Registry Numbers
MDL Number MFCD20720546
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, protected from light

description Product Description

S-Benzyl 2-aminoethanethioate is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. It is often employed in the development of pharmaceutical compounds, particularly in the synthesis of cysteine derivatives and peptide analogs. The compound's thioester and amine functional groups make it valuable for creating sulfur-containing structures, which are crucial in many biologically active molecules. Additionally, it serves as a precursor in the production of ligands for metal coordination chemistry, aiding in the creation of catalysts or materials with specific properties. Its application extends to research in biochemistry, where it is used to study enzyme mechanisms or protein modifications involving thiol groups.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,895.00
inventory 250mg
10-20 days ฿10,008.00
inventory 1g
10-20 days ฿27,000.00

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S-Benzyl 2-aminoethanethioate
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S-Benzyl 2-aminoethanethioate is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. It is often employed in the development of pharmaceutical compounds, particularly in the synthesis of cysteine derivatives and peptide analogs. The compound's thioester and amine functional groups make it valuable for creating sulfur-containing structures, which are crucial in many biologically active molecules. Additionally, it serves as a precursor in the

S-Benzyl 2-aminoethanethioate is primarily utilized in organic synthesis as a versatile building block for the preparation of more complex molecules. It is often employed in the development of pharmaceutical compounds, particularly in the synthesis of cysteine derivatives and peptide analogs. The compound's thioester and amine functional groups make it valuable for creating sulfur-containing structures, which are crucial in many biologically active molecules. Additionally, it serves as a precursor in the production of ligands for metal coordination chemistry, aiding in the creation of catalysts or materials with specific properties. Its application extends to research in biochemistry, where it is used to study enzyme mechanisms or protein modifications involving thiol groups.

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