(S)-Glycidyl 3-nitrobenzenesulfonate

98%

Reagent Code: #234259
label
Alias (2S)-Epoxypropyl m-nitrobenzene sulfonate; (S)-Glycidyl m-nitrobenzene sulfonate; (2S)-Epoxypropyl m-nitrobenzene sulfonate; (S)-(+)-Glycidyl m-nitrobenzene sulfonate
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CAS Number 115314-14-2

science Other reagents with same CAS 115314-14-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.23 g/mol
Formula C₉H₉NO₆S
badge Registry Numbers
MDL Number MFCD00064582
thermostat Physical Properties
Melting Point 61-65 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a chiral building block in organic synthesis, especially in the preparation of enantiomerically pure pharmaceuticals. It serves as an epoxide-opening reagent to introduce functionalized glycidol derivatives in beta-blocker synthesis, such as propranolol and other adrenergic inhibitors. Its activated sulfonate group facilitates nucleophilic attack under mild conditions, enabling efficient coupling with amines or alcohols. Commonly employed in asymmetric synthesis routes where stereochemical control is critical. Also utilized in the development of chiral ligands and catalysts for enantioselective transformations.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿480.00
inventory 25g
10-20 days ฿1,890.00
inventory 100g
10-20 days ฿7,420.00
inventory 500g
10-20 days ฿34,170.00
(S)-Glycidyl 3-nitrobenzenesulfonate
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Used primarily as a chiral building block in organic synthesis, especially in the preparation of enantiomerically pure pharmaceuticals. It serves as an epoxide-opening reagent to introduce functionalized glycidol derivatives in beta-blocker synthesis, such as propranolol and other adrenergic inhibitors. Its activated sulfonate group facilitates nucleophilic attack under mild conditions, enabling efficient coupling with amines or alcohols. Commonly employed in asymmetric synthesis routes where stereochemi

Used primarily as a chiral building block in organic synthesis, especially in the preparation of enantiomerically pure pharmaceuticals. It serves as an epoxide-opening reagent to introduce functionalized glycidol derivatives in beta-blocker synthesis, such as propranolol and other adrenergic inhibitors. Its activated sulfonate group facilitates nucleophilic attack under mild conditions, enabling efficient coupling with amines or alcohols. Commonly employed in asymmetric synthesis routes where stereochemical control is critical. Also utilized in the development of chiral ligands and catalysts for enantioselective transformations.

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