(R)-1-(Tetrahydro-2H-pyran-4-yl)ethan-1-ol

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Reagent Code: #228757
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CAS Number 1568198-40-2

science Other reagents with same CAS 1568198-40-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.18486 g/mol
Formula C₇H₁₄O₂
badge Registry Numbers
MDL Number MFCD21188408
thermostat Physical Properties
Boiling Point 227.7±8.0 °C(Predicted)
inventory_2 Storage & Handling
Density 0.996±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its hydroxyl and ether functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for creating intermediates in drug discovery. Commonly employed in the preparation of protease inhibitors and other bioactive molecules requiring a defined stereocenter. Also utilized in asymmetric synthesis due to its stable chiral center and compatibility with various reaction conditions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿2,790.00
inventory 1g
10-20 days ฿4,750.00
inventory 5g
10-20 days ฿17,570.00
(R)-1-(Tetrahydro-2H-pyran-4-yl)ethan-1-ol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its hydroxyl and ether functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for creating intermediates in drug discovery. Commonly employed in the preparation of protease inhibitors and other bioactive molecules requiring a defined stereocenter. A

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its hydroxyl and ether functional groups allow for further chemical modifications, making it valuable in medicinal chemistry for creating intermediates in drug discovery. Commonly employed in the preparation of protease inhibitors and other bioactive molecules requiring a defined stereocenter. Also utilized in asymmetric synthesis due to its stable chiral center and compatibility with various reaction conditions.

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