(S)-2-methyl-1-(pyridin-2-yl)propan-1-amine

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Reagent Code: #236208
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CAS Number 144852-18-6

science Other reagents with same CAS 144852-18-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 150.22 g/mol
Formula C₉H₁₄N₂
badge Registry Numbers
MDL Number MFCD09257829
thermostat Physical Properties
Boiling Point 226.4±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.979±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its pyridine-containing structure makes it suitable for constructing nitrogen-rich scaffolds found in bioactive molecules. Commonly employed in asymmetric synthesis to introduce chirality, enhancing the selectivity and potency of drug candidates. Also utilized in the development of catalysts for enantioselective transformations due to its stable amine functionality and structural rigidity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,250.00
inventory 250mg
10-20 days ฿27,020.00
inventory 1g
10-20 days ฿54,150.00

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(S)-2-methyl-1-(pyridin-2-yl)propan-1-amine
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its pyridine-containing structure makes it suitable for constructing nitrogen-rich scaffolds found in bioactive molecules. Commonly employed in asymmetric synthesis to introduce chirality, enhancing the selectivity and potency of drug candidates. Also utilized in the development of catalysts for en

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its pyridine-containing structure makes it suitable for constructing nitrogen-rich scaffolds found in bioactive molecules. Commonly employed in asymmetric synthesis to introduce chirality, enhancing the selectivity and potency of drug candidates. Also utilized in the development of catalysts for enantioselective transformations due to its stable amine functionality and structural rigidity.

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