rel-(1S,3R)-3-(2,2,2-Trifluoroacetamido)cyclohexane-1-carboxylicacid

95%

Reagent Code: #237651
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CAS Number 127946-30-9

science Other reagents with same CAS 127946-30-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.19 g/mol
Formula C₉H₁₂F₃NO₃
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and functional groups make it valuable for asymmetric synthesis, enabling the creation of enantiomerically pure drugs. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stability and conformational rigidity provided by the cyclohexane ring. The trifluoroacetamido group enhances metabolic stability and influences binding affinity in target proteins, making this compound useful in designing enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,860.00
inventory 250mg
10-20 days ฿16,690.00
inventory 1g
10-20 days ฿34,120.00

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rel-(1S,3R)-3-(2,2,2-Trifluoroacetamido)cyclohexane-1-carboxylicacid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and functional groups make it valuable for asymmetric synthesis, enabling the creation of enantiomerically pure drugs. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stability and conformational rigidity provided by the cyclohexane ring. The trifluoroacetamido group enhances metabolic

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry and functional groups make it valuable for asymmetric synthesis, enabling the creation of enantiomerically pure drugs. Commonly employed in medicinal chemistry for structure-activity relationship studies due to the stability and conformational rigidity provided by the cyclohexane ring. The trifluoroacetamido group enhances metabolic stability and influences binding affinity in target proteins, making this compound useful in designing enzyme inhibitors.

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