(S)-2-Amino-3-(benzo[d]thiazol-2-yl)propanoic acid hydrochloride

95%

Reagent Code: #38281
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CAS Number 1820581-64-3

science Other reagents with same CAS 1820581-64-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.72 g/mol
Formula C₁₀H₁₁ClN₂O₂S
badge Registry Numbers
MDL Number MFCD27935901
inventory_2 Storage & Handling
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description 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, antimicrobial, and anti-cancer 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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inventory 100mg
10-20 days ฿14,040.00

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(S)-2-Amino-3-(benzo[d]thiazol-2-yl)propanoic acid hydrochloride
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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

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, antimicrobial, and anti-cancer 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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