1-(4,5-Dihydrothiazol-2-yl)azetidine-3-thiol hydrochloride

98%

Reagent Code: #39332
label
Alias 1-(4,5-Dihydrothiazol-2-yl)azetidine-3-thiol hydrochloride; 3-Mercapto-1-(1,3-thiazolin-2-yl)-azepine Cyclobutane-hydrochloride; Tibipenem side chain; Tibipenem side chain; Tibipenem side chain; Tibipenem side chain
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CAS Number 179337-57-6

science Other reagents with same CAS 179337-57-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.75 g/mol
Formula C₆H₁₁ClN₂S₂
thermostat Physical Properties
Melting Point 134-136℃
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzymes or receptors involved in disease pathways. Its structure, featuring a thiazole and azetidine ring, makes it valuable for developing compounds with potential therapeutic applications, such as antimicrobial, antiviral, or anticancer agents. Researchers also explore its use in designing inhibitors for specific proteins or enzymes, leveraging its reactive thiol group for covalent binding or modification. Additionally, it may be employed in the development of prodrugs or as a building block in organic synthesis to create complex molecules with enhanced pharmacological properties.

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Test Parameter Specification
Appearance White to off-white powder or crystals
Purity 97.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,550.00

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1-(4,5-Dihydrothiazol-2-yl)azetidine-3-thiol hydrochloride
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting enzymes or receptors involved in disease pathways. Its structure, featuring a thiazole and azetidine ring, makes it valuable for developing compounds with potential therapeutic applications, such as antimicrobial, antiviral, or anticancer agents. Researchers also explore its use in designing inhibitors for specific proteins or enzymes, leveraging its reactive thiol group for covalent binding or modification. Additionally, it may be employed in the development of prodrugs or as a building block in organic synthesis to create complex molecules with enhanced pharmacological properties.
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