(S)-3-(Allylthio)-2-aminopropanoic acid

≥95%

Reagent Code: #52254
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CAS Number 770742-93-3

science Other reagents with same CAS 770742-93-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 161.22 g/mol
Formula C₆H₁₁NO₂S
badge Registry Numbers
MDL Number MFCD00210474
thermostat Physical Properties
Boiling Point 300.3°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

(S)-3-(Allylthio)-2-aminopropanoic acid is primarily used in the field of biochemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those with potential therapeutic applications. Its structure is valuable in the development of peptide-based drugs, where it can be incorporated to modify the properties of peptides, such as enhancing stability or altering receptor binding affinity. Additionally, it is utilized in studies related to enzyme inhibition, where it can act as a substrate or inhibitor to explore enzymatic mechanisms. This compound is also of interest in the design of prodrugs, where its functional groups can be leveraged to improve drug delivery and bioavailability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,332.00
inventory 1g
10-20 days ฿4,014.00
inventory 100mg
10-20 days ฿792.00

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(S)-3-(Allylthio)-2-aminopropanoic acid
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(S)-3-(Allylthio)-2-aminopropanoic acid is primarily used in the field of biochemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those with potential therapeutic applications. Its structure is valuable in the development of peptide-based drugs, where it can be incorporated to modify the properties of peptides, such as enhancing stability or altering receptor binding affinity. Additionally, it is utilized in studies related to enzyme inhibition, where it can act as a substrate or inhibitor to explore enzymatic mechanisms. This compound is also of interest in the design of prodrugs, where its functional groups can be leveraged to improve drug delivery and bioavailability.
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