(S)-2-Amino-2-(pyridin-2-yl)ethanol dihydrochloride
95%
- Product Code: 60143
CAS:
1269652-00-7
Molecular Weight: | 211.09 g./mol | Molecular Formula: | C₇H₁₂Cl₂N₂O |
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EC Number: | MDL Number: | MFCD20487949 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature, inert gas |
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 neurological and cardiovascular systems. Its structure, featuring both an amino group and a pyridine ring, makes it a versatile building block for designing ligands that interact with specific receptors or enzymes. Additionally, it is employed in the development of chiral compounds, where its stereochemistry plays a crucial role in enhancing the efficacy and selectivity of potential drugs. Researchers also explore its use in creating novel catalysts for asymmetric synthesis, contributing to advancements in organic chemistry and drug discovery.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿7,020.00 |
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0.250 | 10-20 days | ฿13,050.00 |
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(S)-2-Amino-2-(pyridin-2-yl)ethanol dihydrochloride
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 neurological and cardiovascular systems. Its structure, featuring both an amino group and a pyridine ring, makes it a versatile building block for designing ligands that interact with specific receptors or enzymes. Additionally, it is employed in the development of chiral compounds, where its stereochemistry plays a crucial role in enhancing the efficacy and selectivity of potential drugs. Researchers also explore its use in creating novel catalysts for asymmetric synthesis, contributing to advancements in organic chemistry and drug discovery.
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