(R)-(Tetrahydrofuran-3-yl)methanol

98%

Reagent Code: #228658
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CAS Number 124506-31-6

science Other reagents with same CAS 124506-31-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 102.13 g/mol
Formula C₅H₁₀O₂
badge Registry Numbers
MDL Number MFCD17015962
thermostat Physical Properties
Boiling Point 198.6±0.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.038±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring high enantiomeric purity. Its hydroxyl and tetrahydrofuran functional groups make it valuable for constructing complex molecules in medicinal chemistry. Commonly employed in the preparation of protease inhibitors and other bioactive compounds where stereochemistry plays a critical role in biological activity. Also utilized in the synthesis of agrochemicals and specialty polymers due to its structural rigidity and functional handle for further chemical modification.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,770.00
inventory 1g
10-20 days ฿40,210.00
(R)-(Tetrahydrofuran-3-yl)methanol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring high enantiomeric purity. Its hydroxyl and tetrahydrofuran functional groups make it valuable for constructing complex molecules in medicinal chemistry. Commonly employed in the preparation of protease inhibitors and other bioactive compounds where stereochemistry plays a critical role in biological activity. Also utilized in the synthesis of agrochemicals and specialty pol

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active ingredients requiring high enantiomeric purity. Its hydroxyl and tetrahydrofuran functional groups make it valuable for constructing complex molecules in medicinal chemistry. Commonly employed in the preparation of protease inhibitors and other bioactive compounds where stereochemistry plays a critical role in biological activity. Also utilized in the synthesis of agrochemicals and specialty polymers due to its structural rigidity and functional handle for further chemical modification.

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