(S)-2-Amino-3-(benzo[d]thiazol-2-yl)propanoic acid hydrochloride
95%
- Product Code: 38281
CAS:
1820581-64-3
| Molecular Weight: | 258.72 g./mol | Molecular Formula: | C₁₀H₁₁ClN₂O₂S |
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| EC Number: | MDL Number: | MFCD27935901 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a benzo[d]thiazole moiety, makes it a valuable building block for designing molecules with potential therapeutic applications. It is often explored in the development of compounds targeting neurological disorders, as the benzo[d]thiazole group is known to interact with biological systems involved in brain function. Additionally, its chiral nature allows for the creation of enantiomerically pure substances, which is crucial in optimizing drug efficacy and reducing side effects. Researchers also investigate its use in the development of anti-inflammatory and antimicrobial agents due to the bioactive properties of the thiazole ring. Its hydrochloride form enhances solubility, making it suitable for various experimental and formulation purposes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿14,040.00 |
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(S)-2-Amino-3-(benzo[d]thiazol-2-yl)propanoic acid hydrochloride
This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of novel drug candidates. Its structure, featuring a benzo[d]thiazole moiety, makes it a valuable building block for designing molecules with potential therapeutic applications. It is often explored in the development of compounds targeting neurological disorders, as the benzo[d]thiazole group is known to interact with biological systems involved in brain function. Additionally, its chiral nature allows for the creation of enantiomerically pure substances, which is crucial in optimizing drug efficacy and reducing side effects. Researchers also investigate its use in the development of anti-inflammatory and antimicrobial agents due to the bioactive properties of the thiazole ring. Its hydrochloride form enhances solubility, making it suitable for various experimental and formulation purposes.
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