(2R,3R)-2,3-Pentandiol

95%

Reagent Code: #229121
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CAS Number 104870-83-9

science Other reagents with same CAS 104870-83-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 104.15 g/mol
Formula C₅H₁₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its stereochemistry makes it valuable for asymmetric synthesis, where control of molecular handedness is critical. Commonly employed in the development of biologically active compounds, including intermediates for antibiotics and antiviral agents. Also finds use in the synthesis of specialty polymers and ligands for catalysts. Due to its diol functionality, it can act as a precursor in cyclization and condensation reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿25,000.00
(2R,3R)-2,3-Pentandiol
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Used as a chiral building block in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its stereochemistry makes it valuable for asymmetric synthesis, where control of molecular handedness is critical. Commonly employed in the development of biologically active compounds, including intermediates for antibiotics and antiviral agents. Also finds use in the synthesis of specialty polymers and ligands for catalysts. Due to its diol functionality, it can act as a precurso

Used as a chiral building block in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its stereochemistry makes it valuable for asymmetric synthesis, where control of molecular handedness is critical. Commonly employed in the development of biologically active compounds, including intermediates for antibiotics and antiviral agents. Also finds use in the synthesis of specialty polymers and ligands for catalysts. Due to its diol functionality, it can act as a precursor in cyclization and condensation reactions.

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