(S)-3-(Benzyloxy)-2-Hydroxypropyl 4-Methylbenzenesulfonate

95%

Reagent Code: #236159
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CAS Number 16495-04-8

science Other reagents with same CAS 16495-04-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 336.4 g/mol
Formula C₁₇H₂₀O₅S
badge Registry Numbers
MDL Number MFCD00134286
thermostat Physical Properties
Melting Point 52-55 °C
Boiling Point 515.6±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.253±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the preparation of chiral building blocks for pharmaceuticals. Its functional groups allow for selective transformations, making it valuable in asymmetric synthesis. Commonly employed in the development of beta-blockers and other cardiovascular drugs due to its ability to introduce stereochemical control. Also utilized in the preparation of glycerol derivatives and modified nucleosides for antiviral research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,700.00
inventory 250mg
10-20 days ฿12,170.00
inventory 1g
10-20 days ฿24,340.00

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(S)-3-(Benzyloxy)-2-Hydroxypropyl 4-Methylbenzenesulfonate
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the preparation of chiral building blocks for pharmaceuticals. Its functional groups allow for selective transformations, making it valuable in asymmetric synthesis. Commonly employed in the development of beta-blockers and other cardiovascular drugs due to its ability to introduce stereochemical control. Also utilized in the preparation of glycerol derivatives and modified nucleosides for antiviral research.
Used as an intermediate in the synthesis of biologically active compounds, particularly in the preparation of chiral building blocks for pharmaceuticals. Its functional groups allow for selective transformations, making it valuable in asymmetric synthesis. Commonly employed in the development of beta-blockers and other cardiovascular drugs due to its ability to introduce stereochemical control. Also utilized in the preparation of glycerol derivatives and modified nucleosides for antiviral research.
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