N-Boc-(S)-1-amino-2-propanol

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Reagent Code: #71215
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CAS Number 167938-56-9

science Other reagents with same CAS 167938-56-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.23 g/mol
Formula C₈H₁₇NO₃
badge Registry Numbers
MDL Number MFCD04974340
thermostat Physical Properties
Boiling Point 276.4±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.025±0.06 g/cm3(Predicted)
Storage Store at room temperature, away from light, inert atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of chiral compounds and active pharmaceutical ingredients (APIs). It is widely applied in peptide synthesis, where the Boc group serves as a protective group for amines, ensuring selective reactions. Additionally, it plays a role in the development of agrochemicals and fine chemicals, contributing to the creation of enantiomerically pure products. Its chiral nature makes it valuable in asymmetric synthesis, enhancing the efficiency and specificity of chemical processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿12,033.00
inventory 1g
10-20 days ฿1,800.00
inventory 5g
10-20 days ฿3,600.00

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N-Boc-(S)-1-amino-2-propanol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of chiral compounds and active pharmaceutical ingredients (APIs). It is widely applied in peptide synthesis, where the Boc group serves as a protective group for amines, ensuring selective reactions. Additionally, it plays a role in the development of agrochemicals and fine chemicals, contributing to the creation of enantiomerically pure products. Its chiral nature makes it valuable in asymmetric synthesis, enh

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of chiral compounds and active pharmaceutical ingredients (APIs). It is widely applied in peptide synthesis, where the Boc group serves as a protective group for amines, ensuring selective reactions. Additionally, it plays a role in the development of agrochemicals and fine chemicals, contributing to the creation of enantiomerically pure products. Its chiral nature makes it valuable in asymmetric synthesis, enhancing the efficiency and specificity of chemical processes.

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