(R)-2-Methyl-N-((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)propane-2-sulfinamide

≥95%

Reagent Code: #229079
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CAS Number 2230840-35-2

science Other reagents with same CAS 2230840-35-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 338.3459 g/mol
Formula C₁₃H₁₇F₃N₂O₃S
thermostat Physical Properties
Boiling Point 387.7±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.338±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure amines and amino derivatives. Its structure enables high stereoselectivity in nucleophilic addition reactions, making it valuable in pharmaceutical synthesis where specific enantiomers are required for optimal biological activity. Commonly employed in the development of active pharmaceutical ingredients (APIs) due to its ability to direct asymmetric transformations and then be cleanly removed under mild conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿12,800.00
50mg
10-20 days ฿19,200.00
100mg
10-20 days ฿32,000.00
500mg
10-20 days ฿108,800.00
(R)-2-Methyl-N-((R)-1-(3-nitro-5-(trifluoromethyl)phenyl)ethyl)propane-2-sulfinamide
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Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure amines and amino derivatives. Its structure enables high stereoselectivity in nucleophilic addition reactions, making it valuable in pharmaceutical synthesis where specific enantiomers are required for optimal biological activity. Commonly employed in the development of active pharmaceutical ingredients (APIs) due to its ability to direct asymmetric transformations and then be cleanly removed unde

Used as a chiral auxiliary in asymmetric synthesis, particularly in the preparation of enantiomerically pure amines and amino derivatives. Its structure enables high stereoselectivity in nucleophilic addition reactions, making it valuable in pharmaceutical synthesis where specific enantiomers are required for optimal biological activity. Commonly employed in the development of active pharmaceutical ingredients (APIs) due to its ability to direct asymmetric transformations and then be cleanly removed under mild conditions.

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