tert-Butyl 4-(((trifluoromethyl)sulfonyl)oxy)-5,6-dihydropyridine-1(2H)-carboxylate

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Reagent Code: #145924
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CAS Number 138647-49-1

science Other reagents with same CAS 138647-49-1

blur_circular Chemical Specifications

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Weight 331.31 g/mol
Formula C₁₁H₁₆F₃NO₅S
badge Registry Numbers
MDL Number MFCD09997858
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nitrogen-containing heterocyclic drugs. Its structure allows for selective functionalization in medicinal chemistry, making it valuable in creating analogs for drug discovery. Commonly employed in alkylating reactions due to the activated leaving group, enabling efficient formation of substituted piperidine derivatives. Also utilized in agrochemical research for building complex molecules with bioactive properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿310.00
inventory 1g
10-20 days ฿500.00
inventory 5g
10-20 days ฿2,080.00
inventory 25g
10-20 days ฿9,780.00

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tert-Butyl 4-(((trifluoromethyl)sulfonyl)oxy)-5,6-dihydropyridine-1(2H)-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nitrogen-containing heterocyclic drugs. Its structure allows for selective functionalization in medicinal chemistry, making it valuable in creating analogs for drug discovery. Commonly employed in alkylating reactions due to the activated leaving group, enabling efficient formation of substituted piperidine derivatives. Also utilized in agrochemical research for building complex molecules with bioactive
Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of nitrogen-containing heterocyclic drugs. Its structure allows for selective functionalization in medicinal chemistry, making it valuable in creating analogs for drug discovery. Commonly employed in alkylating reactions due to the activated leaving group, enabling efficient formation of substituted piperidine derivatives. Also utilized in agrochemical research for building complex molecules with bioactive properties.
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