(S)-2-Amino-4-((trifluoromethyl)thio)butanoic acid

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Reagent Code: #38291
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CAS Number 764-52-3

science Other reagents with same CAS 764-52-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.18 g/mol
Formula C₅H₈F₃NO₂S
badge Registry Numbers
MDL Number MFCD07636752
thermostat Physical Properties
Boiling Point 260.6°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.45g/cm3
Storage Room temperature, away from light, stored in an inert gas

description Product Description

This compound is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring a trifluoromethylthio group, makes it valuable for designing compounds with enhanced metabolic stability and bioavailability. It is often employed in the creation of potential drug candidates targeting neurological disorders, as the trifluoromethylthio group can influence receptor binding and activity. Additionally, it is used in the study of enzyme mechanisms and as a building block in peptide chemistry, where its chiral center allows for the production of stereospecific compounds. Its applications also extend to agrochemical research, where it contributes to the development of novel pesticides and herbicides with improved efficacy.

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Test Parameter Specification
Appearance White to Off-White Solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 20mg
10-20 days ฿34,490.00

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(S)-2-Amino-4-((trifluoromethyl)thio)butanoic acid
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This compound is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring a trifluoromethylthio group, makes it valuable for designing compounds with enhanced metabolic stability and bioavailability. It is often employed in the creation of potential drug candidates targeting neurological disorders, as the trifluoromethylthio group can influence receptor bindi

This compound is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring a trifluoromethylthio group, makes it valuable for designing compounds with enhanced metabolic stability and bioavailability. It is often employed in the creation of potential drug candidates targeting neurological disorders, as the trifluoromethylthio group can influence receptor binding and activity. Additionally, it is used in the study of enzyme mechanisms and as a building block in peptide chemistry, where its chiral center allows for the production of stereospecific compounds. Its applications also extend to agrochemical research, where it contributes to the development of novel pesticides and herbicides with improved efficacy.

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