Acetic acid (1S,2R)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenylpropyl Ester [Reagent for double aldol reaction]

98%

Reagent Code: #134915
label
Alias (1S,2R)-N-benzyl-N-(methylylsulfonyl)-O-acetyl ephedrine (1S,2R)-2-[N-benzyl-N-(methylylsulfonyl)amino]-1-phenylepropyl acetate
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CAS Number 240423-53-4

science Other reagents with same CAS 240423-53-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 465.61 g/mol
Formula C₂₇H₃₁NO₄S
badge Registry Numbers
MDL Number MFCD02093425
thermostat Physical Properties
Melting Point 121 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, this acetic acid ester derivative enables highly stereoselective double aldol reactions. It facilitates the formation of complex polyol structures with excellent diastereo- and enantiocontrol, making it valuable in the synthesis of natural products and bioactive molecules. The reagent’s bulky mesitylenesulfonyl and benzyl groups help direct stereochemical outcomes by shielding one face of the enolate intermediate. After the desired transformation, the auxiliary can be cleaved under mild conditions, leaving the chiral framework intact. Its application is particularly useful in pharmaceutical research where precise stereochemistry is critical.

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inventory 1g
10-20 days ฿10,680.00

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Acetic acid (1S,2R)-2-[N-Benzyl-N-(mesitylenesulfonyl)amino]-1-phenylpropyl Ester [Reagent for double aldol reaction]
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Used as a chiral auxiliary in asymmetric synthesis, this acetic acid ester derivative enables highly stereoselective double aldol reactions. It facilitates the formation of complex polyol structures with excellent diastereo- and enantiocontrol, making it valuable in the synthesis of natural products and bioactive molecules. The reagent’s bulky mesitylenesulfonyl and benzyl groups help direct stereochemical outcomes by shielding one face of the enolate intermediate. After the desired transformation, the a

Used as a chiral auxiliary in asymmetric synthesis, this acetic acid ester derivative enables highly stereoselective double aldol reactions. It facilitates the formation of complex polyol structures with excellent diastereo- and enantiocontrol, making it valuable in the synthesis of natural products and bioactive molecules. The reagent’s bulky mesitylenesulfonyl and benzyl groups help direct stereochemical outcomes by shielding one face of the enolate intermediate. After the desired transformation, the auxiliary can be cleaved under mild conditions, leaving the chiral framework intact. Its application is particularly useful in pharmaceutical research where precise stereochemistry is critical.

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