1-(4,5-Dihydrothiazol-2-yl)azetidine-3-thiol hydrochloride
98%
- Product Code: 39332
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
CAS:
179337-57-6
Molecular Weight: | 210.75 g./mol | Molecular Formula: | C₆H₁₁ClN₂S₂ |
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EC Number: | MDL Number: | ||
Melting Point: | 134-136℃ | Boiling Point: | |
Density: | Storage Condition: | 2~8℃ |
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.
Product Specification:
Test | Specification |
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APPEARANCE | White to off-white powder or crystals |
PURITY | 97.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿2,550.00 |
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1-(4,5-Dihydrothiazol-2-yl)azetidine-3-thiol hydrochloride
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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