(R)-3-Amino-1,2-propanediol

98%

Reagent Code: #229814
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Alias (R)-3-amino-1,2-propanediol
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CAS Number 66211-46-9

science Other reagents with same CAS 66211-46-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 91.11 g/mol
Formula C₃H₉NO₂
badge Registry Numbers
MDL Number MFCD00798261
thermostat Physical Properties
Melting Point 54-56°C
Boiling Point 117-119 °C0.4 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.175 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of antiviral and antibacterial agents. Its hydroxyl and amino groups allow for easy functionalization, making it valuable in creating complex organic molecules. Commonly employed in the development of protease inhibitors and nucleoside analogs. Also utilized in asymmetric synthesis due to its stereochemical purity, enabling the formation of specific enantiomers in drug intermediates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿1,200.00
inventory 25g
10-20 days ฿5,730.00
(R)-3-Amino-1,2-propanediol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of antiviral and antibacterial agents. Its hydroxyl and amino groups allow for easy functionalization, making it valuable in creating complex organic molecules. Commonly employed in the development of protease inhibitors and nucleoside analogs. Also utilized in asymmetric synthesis due to its stereochemical purity, enabling the formation of specific enantiomers in drug intermediates.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of antiviral and antibacterial agents. Its hydroxyl and amino groups allow for easy functionalization, making it valuable in creating complex organic molecules. Commonly employed in the development of protease inhibitors and nucleoside analogs. Also utilized in asymmetric synthesis due to its stereochemical purity, enabling the formation of specific enantiomers in drug intermediates.

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