(R)-(-)-1-BENZYLOXY-3-(P-TOSYLOXY)-2-PROPANOL

95%

Reagent Code: #230684
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CAS Number 23214-66-6

science Other reagents with same CAS 23214-66-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 336.4 g/mol
Formula C₁₇H₂₀O₅S
thermostat Physical Properties
Melting Point 52-55ºC
inventory_2 Storage & Handling
Density 1.253g/cm3
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of biologically active compounds, particularly in the preparation of pharmaceuticals with beta-adrenergic blocking activity. Its functional groups allow for sequential substitution reactions, enabling the construction of complex molecules with high stereochemical control. Commonly employed in the production of adrenergic agents like (R)-propranolol and related beta-blockers. The presence of both benzyloxy and tosyloxy groups provides selective reactivity, making it valuable in multi-step organic syntheses where regioselectivity and enantiomeric purity are critical.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,000.00
inventory 1g
10-20 days ฿6,000.00
inventory 5g
10-20 days ฿19,180.00
(R)-(-)-1-BENZYLOXY-3-(P-TOSYLOXY)-2-PROPANOL
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Used as a chiral building block in the synthesis of biologically active compounds, particularly in the preparation of pharmaceuticals with beta-adrenergic blocking activity. Its functional groups allow for sequential substitution reactions, enabling the construction of complex molecules with high stereochemical control. Commonly employed in the production of adrenergic agents like (R)-propranolol and related beta-blockers. The presence of both benzyloxy and tosyloxy groups provides selective reactivity,

Used as a chiral building block in the synthesis of biologically active compounds, particularly in the preparation of pharmaceuticals with beta-adrenergic blocking activity. Its functional groups allow for sequential substitution reactions, enabling the construction of complex molecules with high stereochemical control. Commonly employed in the production of adrenergic agents like (R)-propranolol and related beta-blockers. The presence of both benzyloxy and tosyloxy groups provides selective reactivity, making it valuable in multi-step organic syntheses where regioselectivity and enantiomeric purity are critical.

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