(S)-(Tetrahydro-2H-pyran-3-yl)methyl benzoate

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Reagent Code: #232459
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CAS Number 219701-50-5

science Other reagents with same CAS 219701-50-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.26 g/mol
Formula C₁₃H₁₆O₃
badge Registry Numbers
MDL Number MFCD29037440
thermostat Physical Properties
Boiling Point 325.7±15.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.096±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure incorporates a tetrahydropyran ring, which is commonly found in drug molecules due to its metabolic stability and favorable pharmacokinetic properties. The ester functionality allows for further chemical modifications, making it valuable in medicinal chemistry for creating analogs and derivatives. It is often employed in asymmetric synthesis to introduce chirality into target molecules, especially in the preparation of protease inhibitors and other therapeutic agents.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿36,000.00
(S)-(Tetrahydro-2H-pyran-3-yl)methyl benzoate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure incorporates a tetrahydropyran ring, which is commonly found in drug molecules due to its metabolic stability and favorable pharmacokinetic properties. The ester functionality allows for further chemical modifications, making it valuable in medicinal chemistry for creating analogs and derivatives. It is often emplo

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of biologically active compounds where stereochemistry plays a critical role. Its structure incorporates a tetrahydropyran ring, which is commonly found in drug molecules due to its metabolic stability and favorable pharmacokinetic properties. The ester functionality allows for further chemical modifications, making it valuable in medicinal chemistry for creating analogs and derivatives. It is often employed in asymmetric synthesis to introduce chirality into target molecules, especially in the preparation of protease inhibitors and other therapeutic agents.

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