(S)-2-Amino-3-(tert-butylthio)propanoic acid hydrochloride

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Reagent Code: #52369
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CAS Number 200353-65-7

science Other reagents with same CAS 200353-65-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.73 g/mol
Formula C₇H₁₆ClNO₂S
badge Registry Numbers
MDL Number MFCD00135154
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its unique structure, featuring a tert-butylthio group, makes it a valuable intermediate in the creation of molecules targeting specific biological pathways. It is often employed in the design of enzyme inhibitors, where the tert-butylthio moiety can enhance binding affinity and selectivity. Additionally, it is used in peptide chemistry to introduce sulfur-containing functional groups into peptide chains, which can improve stability and bioactivity. The hydrochloride form ensures better solubility and handling in various experimental setups. Its applications extend to studies in medicinal chemistry, where it aids in the exploration of new therapeutic agents for conditions such as cancer, cardiovascular diseases, and neurological disorders.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿288.00
inventory 1g
10-20 days ฿495.00
inventory 100mg
10-20 days ฿486.00
inventory 5g
10-20 days ฿1,512.00

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(S)-2-Amino-3-(tert-butylthio)propanoic acid hydrochloride
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its unique structure, featuring a tert-butylthio group, makes it a valuable intermediate in the creation of molecules targeting specific biological pathways. It is often employed in the design of enzyme inhibitors, where the tert-butylthio moiety can enhance binding affinity and selectivity. Additionally, it is used in peptide chemistry to introduce sulfur-containing fun

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its unique structure, featuring a tert-butylthio group, makes it a valuable intermediate in the creation of molecules targeting specific biological pathways. It is often employed in the design of enzyme inhibitors, where the tert-butylthio moiety can enhance binding affinity and selectivity. Additionally, it is used in peptide chemistry to introduce sulfur-containing functional groups into peptide chains, which can improve stability and bioactivity. The hydrochloride form ensures better solubility and handling in various experimental setups. Its applications extend to studies in medicinal chemistry, where it aids in the exploration of new therapeutic agents for conditions such as cancer, cardiovascular diseases, and neurological disorders.

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