(S)-2,3-Bis(benzyloxy)propan-1-ol

95%

Reagent Code: #236802
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CAS Number 20196-71-8

science Other reagents with same CAS 20196-71-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 272.34 g/mol
Formula C₁₇H₂O₃
badge Registry Numbers
MDL Number MFCD02683556
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a chiral building block in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its stereochemistry and protected alcohol functionalities make it valuable for constructing glycerol derivatives, nucleoside analogs, and bioactive molecules where stereocontrol is critical. Commonly employed in the synthesis of antiviral and anticancer agents due to its ability to mimic glycerol moieties in biologically active compounds. The benzyl groups serve as protecting groups that can be selectively removed under mild conditions, allowing stepwise functionalization of the molecule.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,260.00
inventory 250mg
10-20 days ฿4,690.00
inventory 5g
10-20 days ฿49,500.00
inventory 1g
10-20 days ฿12,140.00
(S)-2,3-Bis(benzyloxy)propan-1-ol
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Used as a chiral building block in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its stereochemistry and protected alcohol functionalities make it valuable for constructing glycerol derivatives, nucleoside analogs, and bioactive molecules where stereocontrol is critical. Commonly employed in the synthesis of antiviral and anticancer agents due to its ability to mimic glycerol moieties in biologically active compounds. The benzyl groups serve as protec

Used as a chiral building block in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its stereochemistry and protected alcohol functionalities make it valuable for constructing glycerol derivatives, nucleoside analogs, and bioactive molecules where stereocontrol is critical. Commonly employed in the synthesis of antiviral and anticancer agents due to its ability to mimic glycerol moieties in biologically active compounds. The benzyl groups serve as protecting groups that can be selectively removed under mild conditions, allowing stepwise functionalization of the molecule.

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