(R)-Glycidyl 3-nitrobenzenesulfonate

98%

Reagent Code: #229857
label
Alias (R)-Glycidyl m-nitrobenzene sulfonate; (R)-Glycidyl m-nitrobenzene sulfonate; (2R)-m-nitrobenzene sulfonate epoxy propylene; (R)-(+)-m-nitrobenzene sulfonate glycidyl ester esters
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CAS Number 115314-17-5

science Other reagents with same CAS 115314-17-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.24 g/mol
Formula C₉H₉NO₆S
badge Registry Numbers
MDL Number MFCD00013436
thermostat Physical Properties
Melting Point 59-63 °C
Boiling Point 432.2 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used primarily as a chiral building block in organic synthesis, this compound serves as an efficient epoxide-opening reagent for the preparation of enantiomerically enriched beta-amino alcohols and other functionalized derivatives. Its activated sulfonate group facilitates nucleophilic attack, making it valuable in the synthesis of pharmaceutical intermediates, particularly in routes requiring stereochemical control. It is also employed in the modification of polymers and in asymmetric catalysis research due to its ability to introduce chiral centers in target molecules.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿750.00
25g
10-20 days ฿3,380.00
100g
10-20 days ฿12,880.00
(R)-Glycidyl 3-nitrobenzenesulfonate
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Used primarily as a chiral building block in organic synthesis, this compound serves as an efficient epoxide-opening reagent for the preparation of enantiomerically enriched beta-amino alcohols and other functionalized derivatives. Its activated sulfonate group facilitates nucleophilic attack, making it valuable in the synthesis of pharmaceutical intermediates, particularly in routes requiring stereochemical control. It is also employed in the modification of polymers and in asymmetric catalysis research

Used primarily as a chiral building block in organic synthesis, this compound serves as an efficient epoxide-opening reagent for the preparation of enantiomerically enriched beta-amino alcohols and other functionalized derivatives. Its activated sulfonate group facilitates nucleophilic attack, making it valuable in the synthesis of pharmaceutical intermediates, particularly in routes requiring stereochemical control. It is also employed in the modification of polymers and in asymmetric catalysis research due to its ability to introduce chiral centers in target molecules.

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