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
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
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
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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